Jump to content

Drosha: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous edit
Content deleted Content added
VisualWikitext
Citation bot (talk | contribs)
Bots
5,430,100 edits
Add: s2cid, author pars. 1-1. Removed parameters. Some additions/deletions were actually parameter name changes. | You can use this bot yourself. Report bugs here. | Suggested by Abductive | Category:Genes on human chromosome 5 | via #UCB_Category
m ref tags fixed
 
(29 intermediate revisions by 16 users not shown)
Line 1: Line 1:
{{short description|Ribonuclease III enzyme}}
{{short description|Ribonuclease III enzyme}}
{{cs1 config|name-list-style=vanc|display-authors=6}}
[[File:5b16 drosha dgcr8.png|thumb|Crystal structure of Drosha and DGCR8, which form the core of the microprocessor complex.]]
{{Infobox_gene}}
{{Infobox_gene}}
'''Drosha''' is a Class 2 [[ribonuclease III]] [[enzyme]] <ref name="Filippov">{{cite journal | vauthors = Filippov V, Solovyev V, Filippova M, Gill SS | title = A novel type of RNase III family proteins in eukaryotes | journal = Gene | volume = 245 | issue = 1 | pages = 213–21 | date = March 2000 | pmid = 10713462 | doi = 10.1016/s0378-1119(99)00571-5 }}</ref> that in humans is encoded by the ''DROSHA'' (formerly ''RNASEN'') [[gene]].<ref name="pmid10713462">{{cite journal | vauthors = Filippov V, Solovyev V, Filippova M, Gill SS | title = A novel type of RNase III family proteins in eukaryotes | journal = Gene | volume = 245 | issue = 1 | pages = 213–21 | date = March 2000 | pmid = 10713462 | pmc = | doi = 10.1016/S0378-1119(99)00571-5 }}</ref><ref>{{cite journal | vauthors = Wu H, Xu H, Miraglia LJ, Crooke ST | title = Human RNase III is a 160-kDa protein involved in preribosomal RNA processing | language = en | journal = The Journal of Biological Chemistry | volume = 275 | issue = 47 | pages = 36957–65 | date = November 2000 | pmid = 10948199 | doi = 10.1074/jbc.M005494200 | doi-access = free }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: RNASEN ribonuclease III, nuclear| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=29102| accessdate = }}</ref>
'''Drosha''' is a Class 2 [[ribonuclease III]] [[enzyme]]<ref name="Filippov">{{cite journal | vauthors = Filippov V, Solovyev V, Filippova M, Gill SS |author-link2=Victor V. Solovyev | title = A novel type of RNase III family proteins in eukaryotes | journal = Gene | volume = 245 | issue = 1 | pages = 213–221 | date = March 2000 | pmid = 10713462 | doi = 10.1016/s0378-1119(99)00571-5 }}</ref> that in humans is encoded by the ''DROSHA'' (formerly ''RNASEN'') [[gene]].<ref name="pmid10713462">{{cite journal | vauthors = Filippov V, Solovyev V, Filippova M, Gill SS | title = A novel type of RNase III family proteins in eukaryotes | journal = Gene | volume = 245 | issue = 1 | pages = 213–221 | date = March 2000 | pmid = 10713462 | doi = 10.1016/S0378-1119(99)00571-5 }}</ref><ref>{{cite journal | vauthors = Wu H, Xu H, Miraglia LJ, Crooke ST | title = Human RNase III is a 160-kDa protein involved in preribosomal RNA processing | journal = The Journal of Biological Chemistry | volume = 275 | issue = 47 | pages = 36957–36965 | date = November 2000 | pmid = 10948199 | doi = 10.1074/jbc.M005494200 | doi-access = free }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: RNASEN ribonuclease III, nuclear| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=29102}}</ref> It is the primary nuclease that executes the initiation step of miRNA processing in the nucleus. It works closely with DGCR8 and in correlation with [[Dicer]]. It has been found significant in clinical knowledge for cancer prognosis.<ref name="pmid19092157" /> and HIV-1 replication.<ref name=":1">{{cite journal | vauthors = Swaminathan G, Navas-Martín S, Martín-García J | title = MicroRNAs and HIV-1 infection: antiviral activities and beyond | journal = Journal of Molecular Biology | volume = 426 | issue = 6 | pages = 1178–97 | date = March 2014 | pmid = 24370931 | doi = 10.1016/j.jmb.2013.12.017 | doi-access = free }}</ref>

== History ==
⚫
Human Drosha was cloned in 2000 when it was identified as a nuclear dsRNA ribonuclease involved in the processing of [[ribosomal RNA]] precursors.<ref name="Lee_2003" /> The other two human enzymes that participate in the processing and activity of miRNA are the [[Dicer]] and [[Argonaute]] proteins. Recently, proteins like Drosha have been found significant in cancer prognosis<ref name="pmid19092157" /> and HIV-1 replication.<ref name=":1" />


== Function ==
== Function ==


Members of the ribonuclease III superfamily of [[double-stranded]] (ds) [[RNA]]-specific [[endoribonuclease]]s participate in diverse [[RNA]] maturation and decay pathways in [[eukaryotic]] and [[prokaryotic]] cells.<ref name=fortin>{{cite journal | vauthors = Fortin KR, Nicholson RH, Nicholson AW | title = Mouse ribonuclease III. cDNA structure, expression analysis, and chromosomal location | journal = BMC Genomics | volume = 3 | issue = 1 | pages = 26 | date = August 2002 | pmid = 12191433 | pmc = 122089 | doi = 10.1186/1471-2164-3-26 }}</ref> The RNase III Drosha is the core [[nuclease]] that executes the initiation step of [[microRNA]] (miRNA) processing in the [[Cell nucleus|nucleus]].<ref name="entrez" /><ref name="Lee_2003">{{cite journal | vauthors = Lee Y, Ahn C, Han J, Choi H, Kim J, Yim J, Lee J, Provost P, Rådmark O, Kim S, Kim VN | title = The nuclear RNase III Drosha initiates microRNA processing | journal = Nature | volume = 425 | issue = 6956 | pages = 415–9 | date = September 2003 | pmid = 14508493 | doi = 10.1038/nature01957 | s2cid = 4421030 }}</ref>
Members of the ribonuclease III superfamily of [[double-stranded]] (ds) [[RNA]]-specific [[endoribonuclease]]s participate in diverse [[RNA]] maturation and decay pathways in [[eukaryotic]] and [[prokaryotic]] cells.<ref name=fortin>{{cite journal | vauthors = Fortin KR, Nicholson RH, Nicholson AW | title = Mouse ribonuclease III. cDNA structure, expression analysis, and chromosomal location | journal = BMC Genomics | volume = 3 | issue = 1 | pages = 26 | date = August 2002 | pmid = 12191433 | pmc = 122089 | doi = 10.1186/1471-2164-3-26 | doi-access = free }}</ref> The '''RNase III Drosha''' is the core [[nuclease]] that executes the initiation step of [[microRNA]] (miRNA) processing in the [[Cell nucleus|nucleus]].<ref name="entrez" /><ref name="Lee_2003">{{cite journal | vauthors = Lee Y, Ahn C, Han J, Choi H, Kim J, Yim J, Lee J, Provost P, Rådmark O, Kim S, Kim VN | title = The nuclear RNase III Drosha initiates microRNA processing | journal = Nature | volume = 425 | issue = 6956 | pages = 415–419 | date = September 2003 | pmid = 14508493 | doi = 10.1038/nature01957 | s2cid = 4421030 | bibcode = 2003Natur.425..415L }}</ref>


The microRNAs thus generated are short [[RNA]] molecules that regulate a wide variety of other genes by interacting with the [[RNA-induced silencing complex]] (RISC) to induce cleavage of [[base pair|complementary]] [[messenger RNA]] (mRNA) as part of the [[RNA interference]] pathway. A microRNA molecule is synthesized as a long RNA [[primary transcript]] known as a ''pri-miRNA'', which is cleaved by Drosha to produce a characteristic [[stem-loop]] structure of about 70 [[base pair]]s long, known as a ''pre-miRNA.''<ref name="Lee_2003"/> Drosha exists as part of a [[protein complex]] called the [[Microprocessor complex]], which also contains the double-stranded RNA binding protein [[DGCR8]] (called [[Pasha (protein)|Pasha]] in ''[[Drosophila | D. melanogaster]]'' and ''[[Caenorhabditis_elegans | C. elegans]]'').<ref name="pmid15531879">{{cite journal | vauthors = Denli AM, Tops BB, Plasterk RH, Ketting RF, Hannon GJ | title = Processing of primary microRNAs by the Microprocessor complex | journal = Nature | volume = 432 | issue = 7014 | pages = 231–5 | date = November 2004 | pmid = 15531879 | doi = 10.1038/nature03049 | s2cid = 4425505 }}</ref> DGCR8 is essential for Drosha activity and is capable of binding single-stranded fragments of the pri-miRNA that are required for proper processing.<ref name="pmid16751099">{{cite journal | vauthors = Han J, Lee Y, Yeom KH, Nam JW, Heo I, Rhee JK, Sohn SY, Cho Y, Zhang BT, Kim VN | title = Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex | journal = Cell | volume = 125 | issue = 5 | pages = 887–901 | date = June 2006 | pmid = 16751099 | doi = 10.1016/j.cell.2006.03.043 | s2cid = 453021 }}</ref>
The microRNAs thus generated are short [[RNA]] molecules that regulate a wide variety of other genes by interacting with the [[RNA-induced silencing complex]] (RISC) to induce cleavage of [[base pair|complementary]] [[messenger RNA]] (mRNA) as part of the [[RNA interference]] pathway. MicroRNA molecules are synthesized as long RNA [[primary transcript]]s known as a ''pri-miRNAs'', which are cleaved by Drosha to produce a characteristic [[stem-loop]] structure of about 70 [[base pair]]s long, known as a ''pre-miRNA.''<ref name="Lee_2003"/> Pre-miRNAs, when associated with EXP5, are stabilized due to removal of the 5' cap and 3' poly(A) tail.<ref name="pmid26434509">{{cite journal | vauthors = Sloan KE, Gleizes PE, Bohnsack MT | title = Nucleocytoplasmic Transport of RNAs and RNA-Protein Complexes | journal = Journal of Molecular Biology | volume = 428 | issue = 10 Pt A | pages = 2040–59 | date = May 2016 | pmid = 26434509 | doi = 10.1016/j.jmb.2015.09.023 | url = }}</ref> Drosha exists as part of a [[protein complex]] called the [[Microprocessor complex]], which also contains the double-stranded RNA binding protein [[DGCR8]] (called [[Pasha (protein)|Pasha]] in ''[[Drosophila|D. melanogaster]]'' and ''[[Caenorhabditis elegans|C. elegans]]'').<ref name="pmid15531879">{{cite journal | vauthors = Denli AM, Tops BB, Plasterk RH, Ketting RF, Hannon GJ | title = Processing of primary microRNAs by the Microprocessor complex | journal = Nature | volume = 432 | issue = 7014 | pages = 231–235 | date = November 2004 | pmid = 15531879 | doi = 10.1038/nature03049 | s2cid = 4425505 | bibcode = 2004Natur.432..231D }}</ref> DGCR8 is essential for Drosha activity and is capable of binding single-stranded fragments of the pri-miRNA that are required for proper processing.<ref name="pmid16751099">{{cite journal | vauthors = Han J, Lee Y, Yeom KH, Nam JW, Heo I, Rhee JK, Sohn SY, Cho Y, Zhang BT, Kim VN | title = Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex | journal = Cell | volume = 125 | issue = 5 | pages = 887–901 | date = June 2006 | pmid = 16751099 | doi = 10.1016/j.cell.2006.03.043 | s2cid = 453021 | doi-access = free }}</ref> The Drosha complex also contains several auxiliary factors such as [[RNA-binding protein EWS|EWSR1]], FUS, [[Heterogeneous ribonucleoprotein particle|hnRNPs]], p68, and p72.<ref name=":2" />


⚫
Both Drosha and DGCR8 are localized to the [[cell nucleus]], where processing of pri-miRNA to pre-miRNA occurs. These two proteins homeostatically control miRNA biogenesis by an auto-feedback loop.<ref name=":2" /> A 2nt 3' overhang is generated by Drosha in the nucleus recognized by [[Dicer]] in the cytoplasm, which couples the upstream and downstream processing events. Pre-miRNA is then further processed by the RNase [[Dicer]] into mature miRNAs in the cell [[cytoplasm]].<ref name="Lee_2003" /><ref name=":2" /> There also exists an isoform of Drosha that does not contain a nuclear localization signal, which results in the generation of c-Drosha.<ref name="LINK">{{cite journal | vauthors = Link S, Grund SE, Diederichs S | title = Alternative splicing affects the subcellular localization of Drosha | journal = Nucleic Acids Research | volume = 44 | issue = 11 | pages = 5330–5343 | date = June 2016 | pmid = 27185895 | pmc = 4914122 | doi = 10.1093/nar/gkw400 }}</ref><ref name="nar.oxfordjournals.org">{{cite journal | vauthors = Dai L, Chen K, Youngren B, Kulina J, Yang A, Guo Z, Li J, Yu P, Gu S | title = Cytoplasmic Drosha activity generated by alternative splicing | journal = Nucleic Acids Research | volume = 44 | issue = 21 | pages = 10454–10466 | date = December 2016 | pmid = 27471035 | pmc = 5137420 | doi = 10.1093/nar/gkw668 }}</ref> This variant has been shown to localize to the cell [[cytoplasm]] rather than the nucleus, but the effects on pri-miRNA processing are yet unclear.
⚫
Human Drosha was cloned in 2000 {{Citation needed|date=July 2019}}, when it was identified as a nuclear dsRNA ribonuclease involved in the processing of [[ribosomal RNA]] precursors. The other two human enzymes that participate in the processing and activity of miRNA are the [[Dicer]] and [[Argonaute]] proteins.


⚫
Both Drosha and Dicer also participate in the [[DNA repair|DNA damage response]].<ref name="francia">{{cite journal | vauthors = Francia S, Michelini F, Saxena A, Tang D, de Hoon M, Anelli V, Mione M, Carninci P, d'Adda di Fagagna F | title = Site-specific DICER and DROSHA RNA products control the DNA-damage response | journal = Nature | volume = 488 | issue = 7410 | pages = 231–235 | date = August 2012 | pmid = 22722852 | pmc = 3442236 | doi = 10.1038/nature11179 | bibcode = 2012Natur.488..231F }}</ref>
⚫
Both Drosha and DGCR8 are localized to the [[cell nucleus]], where processing of pri-miRNA to pre-miRNA occurs. This latter molecule is then further processed by the RNase [[Dicer]] into mature miRNAs in the cell [[cytoplasm]].<ref name="Lee_2003" /> There also exists an isoform of Drosha that does not contain a nuclear localization signal, which results in the generation of c-Drosha.<ref name="LINK">{{cite journal | vauthors = Link S, Grund SE, Diederichs S | title = Alternative splicing affects the subcellular localization of Drosha | language = en | journal = Nucleic Acids Research | date = May 2016 | pmid = 27185895 | pmc = 4914122 | doi = 10.1093/nar/gkw400 | volume = 44 | issue = 11 | pages = 5330–43}}</ref><ref name="nar.oxfordjournals.org">{{cite journal | vauthors = Dai L, Chen K, Youngren B, Kulina J, Yang A, Guo Z, Li J, Yu P, Gu S | title = Cytoplasmic Drosha activity generated by alternative splicing | language = en | journal = Nucleic Acids Research | volume = 44 | issue = 21 | date = July 2016 | pmid = 27471035 | pmc = 5137420 | doi = 10.1093/nar/gkw668 | url = http://nar.oxfordjournals.org/content/early/2016/07/28/nar.gkw668 | pages=10454–10466}}</ref> This variant has been shown to localize to the cell [[cytoplasm]] rather than the nucleus, but the effects on pri-miRNA processing are yet unclear.


Certain miRNAs have been found to deviate from conventional biogenesis pathways and do not necessarily require Drosha or [[Dicer]], which is because they do not require the processing of pri-miRNA to pre-miRNA.<ref name=":2">{{cite journal | vauthors = Suzuki HI, Miyazono K | title = Emerging complexity of microRNA generation cascades | journal = Journal of Biochemistry | volume = 149 | issue = 1 | pages = 15–25 | date = January 2011 | pmid = 20876186 | doi = 10.1093/jb/mvq113 }}</ref> Drosha-independent miRNAs derive from [[mirtron]]s, which are genes that encode for miRNAs in their introns and make use of splicing to bypass Drosha cleavage. Simtrons are mirtron-like, splicing-independent, and do require Drosha mediated cleavage, although they do not require most proteins in the canonical pathway such as [[Microprocessor complex subunit DGCR8|DGCR8]] or [[Dicer]].<ref name=":1" />
⚫
Both Drosha and Dicer also participate in the [[DNA repair|DNA damage response]].<ref name="francia">{{cite journal | vauthors = Francia S, Michelini F, Saxena A, Tang D, de Hoon M, Anelli V, Mione M, Carninci P, d'Adda di Fagagna F | title = Site-specific DICER and DROSHA RNA products control the DNA-damage response | journal = Nature | volume = 488 | issue = 7410 | pages = 231–5 | date = August 2012 | pmid = 22722852 | doi = 10.1038/nature11179 | pmc=3442236}}</ref>


== Clinical significance ==
== Clinical significance ==


Drosha and other miRNA processing enzymes may be important in cancer prognosis.<ref name="pmid19092157">{{cite journal | vauthors = Slack FJ, Weidhaas JB | title = MicroRNA in cancer prognosis | journal = The New England Journal of Medicine | volume = 359 | issue = 25 | pages = 2720–2 | date = December 2008 | pmid = 19092157 | doi = 10.1056/NEJMe0808667 }}</ref> Both Drosha and [[Dicer]] can function as [[master regulator]]s of miRNA processing and have been observed to be down-regulated in some types of [[breast cancer]].<ref>{{cite journal | vauthors = Thomson JM, Newman M, Parker JS, Morin-Kensicki EM, Wright T, Hammond SM | title = Extensive post-transcriptional regulation of microRNAs and its implications for cancer | journal = Genes & Development | volume = 20 | issue = 16 | pages = 2202–7 | date = August 2006 | pmid = 16882971 | pmc = 1553203 | doi = 10.1101/gad.1444406 }}</ref> The alternative splicing patterns of Drosha in [[The Cancer Genome Atlas]] have also indicated that c-drosha appears to be enriched in various types of breast cancer, [[Colorectal cancer|colon cancer]], and [[Esophageal cancer|esophagus cancer]].<ref name="nar.oxfordjournals.org"/> However, the exact nature of the association between microRNA processing and [[tumorigenesis]] is unclear,<ref>{{cite journal | vauthors = Iorio MV, Croce CM | title = microRNA involvement in human cancer | journal = Carcinogenesis | volume = 33 | issue = 6 | pages = 1126–33 | date = June 2012 | pmid = 22491715 | doi = 10.1093/carcin/bgs140 | pmc=3514864}}</ref> but its function can be effectively examined by siRNA knockdown based on an independent validation.<ref>{{Cite journal|last1=Munkácsy|first1=Gyöngyi|last2=Sztupinszki|first2=Zsófia|last3=Herman|first3=Péter|last4=Bán|first4=Bence|last5=Pénzváltó|first5=Zsófia|last6=Szarvas|first6=Nóra|last7=Győrffy|first7=Balázs|date=2016-01-01|title=Validation of RNAi Silencing Efficiency Using Gene Array Data shows 18.5% Failure Rate across 429 Independent Experiments|journal=Molecular Therapy - Nucleic Acids|language=English|volume=5|issue=9|pages=e366|doi=10.1038/mtna.2016.66|issn=2162-2531|pmc=5056990|pmid=27673562}}</ref>
Drosha and other miRNA processing enzymes may be important in cancer prognosis.<ref name="pmid19092157">{{cite journal | vauthors = Slack FJ, Weidhaas JB | title = MicroRNA in cancer prognosis | journal = The New England Journal of Medicine | volume = 359 | issue = 25 | pages = 2720–2722 | date = December 2008 | pmid = 19092157 | pmc = 10035200 | doi = 10.1056/NEJMe0808667 }}</ref> Both Drosha and [[Dicer]] can function as [[master regulator]]s of miRNA processing and have been observed to be down-regulated in some types of [[breast cancer]].<ref>{{cite journal | vauthors = Thomson JM, Newman M, Parker JS, Morin-Kensicki EM, Wright T, Hammond SM | title = Extensive post-transcriptional regulation of microRNAs and its implications for cancer | journal = Genes & Development | volume = 20 | issue = 16 | pages = 2202–2207 | date = August 2006 | pmid = 16882971 | pmc = 1553203 | doi = 10.1101/gad.1444406 }}</ref> The alternative splicing patterns of Drosha in [[The Cancer Genome Atlas]] have also indicated that c-drosha appears to be enriched in various types of breast cancer, [[Colorectal cancer|colon cancer]], and [[esophageal cancer]].<ref name="nar.oxfordjournals.org"/> However, the exact nature of the association between microRNA processing and [[tumorigenesis]] is unclear,<ref>{{cite journal | vauthors = Iorio MV, Croce CM | title = microRNA involvement in human cancer | journal = Carcinogenesis | volume = 33 | issue = 6 | pages = 1126–1133 | date = June 2012 | pmid = 22491715 | pmc = 3514864 | doi = 10.1093/carcin/bgs140 }}</ref> but its function can be effectively examined by siRNA knockdown based on an independent validation.<ref>{{cite journal | vauthors = Munkácsy G, Sztupinszki Z, Herman P, Bán B, Pénzváltó Z, Szarvas N, Győrffy B | title = Validation of RNAi Silencing Efficiency Using Gene Array Data shows 18.5% Failure Rate across 429 Independent Experiments | journal = Molecular Therapy. Nucleic Acids | volume = 5 | issue = 9 | pages = e366 | date = September 2016 | pmid = 27673562 | pmc = 5056990 | doi = 10.1038/mtna.2016.66 }}</ref>

Drosha and other miRNA processing enzymes may also be important in HIV-1 replication. miRNAs contribute to the innate antiviral defense. This can be shown by the knockdown of two important miRNA processing proteins, Drosha and Dicer, which leads to a significant enhancement of viral replication in PBMCs from HIV-1-infected patients. Thus, Drosha, in conjunction with Dicer, seem to have a role in controlling HIV-1 replication.<ref name=":1" />
{{Clear}}
{{Clear}}


Line 25: Line 32:
== Further reading ==
== Further reading ==
{{refbegin|33em}}
{{refbegin|33em}}
* {{cite journal | vauthors = Gunther M, Laithier M, Brison O | title = A set of proteins interacting with transcription factor Sp1 identified in a two-hybrid screening | journal = Molecular and Cellular Biochemistry | volume = 210 | issue = 1–2 | pages = 131–42 | date = July 2000 | pmid = 10976766 | doi = 10.1023/A:1007177623283 | s2cid = 1339642 }}
* {{cite journal | vauthors = Gunther M, Laithier M, Brison O | title = A set of proteins interacting with transcription factor Sp1 identified in a two-hybrid screening | journal = Molecular and Cellular Biochemistry | volume = 210 | issue = 1–2 | pages = 131–142 | date = July 2000 | pmid = 10976766 | doi = 10.1023/A:1007177623283 | s2cid = 1339642 }}
* {{cite journal | vauthors = Fortin KR, Nicholson RH, Nicholson AW | title = Mouse ribonuclease III. cDNA structure, expression analysis, and chromosomal location | journal = BMC Genomics | volume = 3 | issue = 1 | pages = 26 | date = August 2002 | pmid = 12191433 | pmc = 122089 | doi = 10.1186/1471-2164-3-26 }}
* {{cite journal | vauthors = Fortin KR, Nicholson RH, Nicholson AW | title = Mouse ribonuclease III. cDNA structure, expression analysis, and chromosomal location | journal = BMC Genomics | volume = 3 | issue = 1 | pages = 26 | date = August 2002 | pmid = 12191433 | pmc = 122089 | doi = 10.1186/1471-2164-3-26 | doi-access = free }}
* {{cite journal | vauthors = Lee Y, Ahn C, Han J, Choi H, Kim J, Yim J, Lee J, Provost P, Rådmark O, Kim S, Kim VN | title = The nuclear RNase III Drosha initiates microRNA processing | journal = Nature | volume = 425 | issue = 6956 | pages = 415–9 | date = September 2003 | pmid = 14508493 | doi = 10.1038/nature01957 | s2cid = 4421030 }}
* {{cite journal | vauthors = Lee Y, Ahn C, Han J, Choi H, Kim J, Yim J, Lee J, Provost P, Rådmark O, Kim S, Kim VN | title = The nuclear RNase III Drosha initiates microRNA processing | journal = Nature | volume = 425 | issue = 6956 | pages = 415–419 | date = September 2003 | pmid = 14508493 | doi = 10.1038/nature01957 | s2cid = 4421030 | bibcode = 2003Natur.425..415L }}
* {{cite journal | vauthors = Gregory RI, Yan KP, Amuthan G, Chendrimada T, Doratotaj B, Cooch N, Shiekhattar R | title = The Microprocessor complex mediates the genesis of microRNAs | journal = Nature | volume = 432 | issue = 7014 | pages = 235–40 | date = November 2004 | pmid = 15531877 | doi = 10.1038/nature03120 | s2cid = 4389261 }}
* {{cite journal | vauthors = Gregory RI, Yan KP, Amuthan G, Chendrimada T, Doratotaj B, Cooch N, Shiekhattar R | title = The Microprocessor complex mediates the genesis of microRNAs | journal = Nature | volume = 432 | issue = 7014 | pages = 235–240 | date = November 2004 | pmid = 15531877 | doi = 10.1038/nature03120 | s2cid = 4389261 | bibcode = 2004Natur.432..235G }}
* {{cite journal | vauthors = Zeng Y, Yi R, Cullen BR | title = Recognition and cleavage of primary microRNA precursors by the nuclear processing enzyme Drosha | journal = The EMBO Journal | volume = 24 | issue = 1 | pages = 138–48 | date = January 2005 | pmid = 15565168 | pmc = 544904 | doi = 10.1038/sj.emboj.7600491 }}
* {{cite journal | vauthors = Zeng Y, Yi R, Cullen BR | title = Recognition and cleavage of primary microRNA precursors by the nuclear processing enzyme Drosha | journal = The EMBO Journal | volume = 24 | issue = 1 | pages = 138–148 | date = January 2005 | pmid = 15565168 | pmc = 544904 | doi = 10.1038/sj.emboj.7600491 }}
* {{cite journal | vauthors = Han J, Lee Y, Yeom KH, Kim YK, Jin H, Kim VN | title = The Drosha-DGCR8 complex in primary microRNA processing | journal = Genes & Development | volume = 18 | issue = 24 | pages = 3016–27 | date = December 2004 | pmid = 15574589 | pmc = 535913 | doi = 10.1101/gad.1262504 }}
* {{cite journal | vauthors = Han J, Lee Y, Yeom KH, Kim YK, Jin H, Kim VN | title = The Drosha-DGCR8 complex in primary microRNA processing | journal = Genes & Development | volume = 18 | issue = 24 | pages = 3016–3027 | date = December 2004 | pmid = 15574589 | pmc = 535913 | doi = 10.1101/gad.1262504 }}
* {{cite journal | vauthors = Landthaler M, Yalcin A, Tuschl T | title = The human DiGeorge syndrome critical region gene 8 and Its D. melanogaster homolog are required for miRNA biogenesis | journal = Current Biology | volume = 14 | issue = 23 | pages = 2162–7 | date = December 2004 | pmid = 15589161 | doi = 10.1016/j.cub.2004.11.001 | hdl = 11858/00-001M-0000-0012-EB83-3 | s2cid = 13266269 | hdl-access = free }}
* {{cite journal | vauthors = Landthaler M, Yalcin A, Tuschl T | title = The human DiGeorge syndrome critical region gene 8 and Its D. melanogaster homolog are required for miRNA biogenesis | journal = Current Biology | volume = 14 | issue = 23 | pages = 2162–2167 | date = December 2004 | pmid = 15589161 | doi = 10.1016/j.cub.2004.11.001 | bibcode = 2004CBio...14.2162L | hdl-access = free | s2cid = 13266269 | hdl = 11858/00-001M-0000-0012-EB83-3 }}
* {{cite journal | vauthors = Zeng Y, Cullen BR | title = Efficient processing of primary microRNA hairpins by Drosha requires flanking nonstructured RNA sequences | journal = The Journal of Biological Chemistry | volume = 280 | issue = 30 | pages = 27595–603 | date = July 2005 | pmid = 15932881 | doi = 10.1074/jbc.M504714200 | doi-access = free }}
* {{cite journal | vauthors = Zeng Y, Cullen BR | title = Efficient processing of primary microRNA hairpins by Drosha requires flanking nonstructured RNA sequences | journal = The Journal of Biological Chemistry | volume = 280 | issue = 30 | pages = 27595–27603 | date = July 2005 | pmid = 15932881 | doi = 10.1074/jbc.M504714200 | doi-access = free }}
* {{cite journal | vauthors = Irvin-Wilson CV, Chaudhuri G | title = Alternative initiation and splicing in dicer gene expression in human breast cells | journal = Breast Cancer Research | volume = 7 | issue = 4 | pages = R563–9 | year = 2006 | pmid = 15987463 | pmc = 1175071 | doi = 10.1186/bcr1043 }}
* {{cite journal | vauthors = Irvin-Wilson CV, Chaudhuri G | title = Alternative initiation and splicing in dicer gene expression in human breast cells | journal = Breast Cancer Research | volume = 7 | issue = 4 | pages = R563–R569 | year = 2006 | pmid = 15987463 | pmc = 1175071 | doi = 10.1186/bcr1043 | doi-access = free }}
* {{cite journal | vauthors = Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T, Sugano S | title = Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes | journal = Genome Research | volume = 16 | issue = 1 | pages = 55–65 | date = January 2006 | pmid = 16344560 | pmc = 1356129 | doi = 10.1101/gr.4039406 }}
* {{cite journal | vauthors = Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T, Sugano S | title = Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes | journal = Genome Research | volume = 16 | issue = 1 | pages = 55–65 | date = January 2006 | pmid = 16344560 | pmc = 1356129 | doi = 10.1101/gr.4039406 }}
* {{cite journal | vauthors = Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M | title = Global, in vivo, and site-specific phosphorylation dynamics in signaling networks | journal = Cell | volume = 127 | issue = 3 | pages = 635–48 | date = November 2006 | pmid = 17081983 | doi = 10.1016/j.cell.2006.09.026 | s2cid = 7827573 }}
* {{cite journal | vauthors = Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M | title = Global, in vivo, and site-specific phosphorylation dynamics in signaling networks | journal = Cell | volume = 127 | issue = 3 | pages = 635–648 | date = November 2006 | pmid = 17081983 | doi = 10.1016/j.cell.2006.09.026 | s2cid = 7827573 | doi-access = free }}
* {{cite journal | vauthors = Sugito N, Ishiguro H, Kuwabara Y, Kimura M, Mitsui A, Kurehara H, Ando T, Mori R, Takashima N, Ogawa R, Fujii Y | title = RNASEN regulates cell proliferation and affects survival in esophageal cancer patients | journal = Clinical Cancer Research | volume = 12 | issue = 24 | pages = 7322–8 | date = December 2006 | pmid = 17121874 | doi = 10.1158/1078-0432.CCR-06-0515 | doi-access = free }}
* {{cite journal | vauthors = Sugito N, Ishiguro H, Kuwabara Y, Kimura M, Mitsui A, Kurehara H, Ando T, Mori R, Takashima N, Ogawa R, Fujii Y | title = RNASEN regulates cell proliferation and affects survival in esophageal cancer patients | journal = Clinical Cancer Research | volume = 12 | issue = 24 | pages = 7322–7328 | date = December 2006 | pmid = 17121874 | doi = 10.1158/1078-0432.CCR-06-0515 | s2cid = 7569257 | doi-access = }}
* {{cite journal | vauthors = Kim YK, Kim VN | title = Processing of intronic microRNAs | journal = The EMBO Journal | volume = 26 | issue = 3 | pages = 775–83 | date = February 2007 | pmid = 17255951 | pmc = 1794378 | doi = 10.1038/sj.emboj.7601512 }}
* {{cite journal | vauthors = Kim YK, Kim VN | title = Processing of intronic microRNAs | journal = The EMBO Journal | volume = 26 | issue = 3 | pages = 775–783 | date = February 2007 | pmid = 17255951 | pmc = 1794378 | doi = 10.1038/sj.emboj.7601512 }}
* {{cite journal | vauthors = Xing L, Kieff E | title = Epstein-Barr virus BHRF1 micro- and stable RNAs during latency III and after induction of replication | journal = Journal of Virology | volume = 81 | issue = 18 | pages = 9967–75 | date = September 2007 | pmid = 17626073 | pmc = 2045418 | doi = 10.1128/JVI.02244-06 }}
* {{cite journal | vauthors = Xing L, Kieff E | title = Epstein-Barr virus BHRF1 micro- and stable RNAs during latency III and after induction of replication | journal = Journal of Virology | volume = 81 | issue = 18 | pages = 9967–9975 | date = September 2007 | pmid = 17626073 | pmc = 2045418 | doi = 10.1128/JVI.02244-06 }}
{{refend}}
{{refend}}


== External links ==
== External links ==
* {{PDBe-KB2|Q9NRR4|Ribonuclease 3}}
* {{PDBe-KB2|Q9NRR4|Ribonuclease 3}}



[[Category:Ribonucleases]]
[[Category:Ribonucleases]]

Latest revision as of 09:27, 12 November 2024

Crystal structure of Drosha and DGCR8, which form the core of the microprocessor complex.
DROSHA
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesDROSHA, ETOHI2, HSA242976, RANSE3L, RN3, RNASE3L, RNASEN, drosha ribonuclease III
External IDsOMIM: 608828; MGI: 1261425; HomoloGene: 8293; GeneCards: DROSHA; OMA:DROSHA - orthologs
Orthologs
SpeciesHumanMouse
Entrez

29102

14000

Ensembl

ENSG00000113360

ENSMUSG00000022191

UniProt

Q9NRR4

Q5HZJ0

RefSeq (mRNA)

NM_001100412
NM_013235
NM_001382508

NM_001130149
NM_026799

RefSeq (protein)

NP_001093882
NP_037367
NP_001369437

NP_001123621
NP_081075

Location (UCSC)Chr 5: 31.4 – 31.53 MbChr 15: 12.82 – 12.94 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Drosha is a Class 2 ribonuclease III enzyme[5] that in humans is encoded by the DROSHA (formerly RNASEN) gene.[6][7][8] It is the primary nuclease that executes the initiation step of miRNA processing in the nucleus. It works closely with DGCR8 and in correlation with Dicer. It has been found significant in clinical knowledge for cancer prognosis.[9] and HIV-1 replication.[10]

History

[edit]

Human Drosha was cloned in 2000 when it was identified as a nuclear dsRNA ribonuclease involved in the processing of ribosomal RNA precursors.[11] The other two human enzymes that participate in the processing and activity of miRNA are the Dicer and Argonaute proteins. Recently, proteins like Drosha have been found significant in cancer prognosis[9] and HIV-1 replication.[10]

Function

[edit]

Members of the ribonuclease III superfamily of double-stranded (ds) RNA-specific endoribonucleases participate in diverse RNA maturation and decay pathways in eukaryotic and prokaryotic cells.[12] The RNase III Drosha is the core nuclease that executes the initiation step of microRNA (miRNA) processing in the nucleus.[8][11]

The microRNAs thus generated are short RNA molecules that regulate a wide variety of other genes by interacting with the RNA-induced silencing complex (RISC) to induce cleavage of complementary messenger RNA (mRNA) as part of the RNA interference pathway. MicroRNA molecules are synthesized as long RNA primary transcripts known as a pri-miRNAs, which are cleaved by Drosha to produce a characteristic stem-loop structure of about 70 base pairs long, known as a pre-miRNA.[11] Pre-miRNAs, when associated with EXP5, are stabilized due to removal of the 5' cap and 3' poly(A) tail.[13] Drosha exists as part of a protein complex called the Microprocessor complex, which also contains the double-stranded RNA binding protein DGCR8 (called Pasha in D. melanogaster and C. elegans).[14] DGCR8 is essential for Drosha activity and is capable of binding single-stranded fragments of the pri-miRNA that are required for proper processing.[15] The Drosha complex also contains several auxiliary factors such as EWSR1, FUS, hnRNPs, p68, and p72.[16]

Both Drosha and DGCR8 are localized to the cell nucleus, where processing of pri-miRNA to pre-miRNA occurs. These two proteins homeostatically control miRNA biogenesis by an auto-feedback loop.[16] A 2nt 3' overhang is generated by Drosha in the nucleus recognized by Dicer in the cytoplasm, which couples the upstream and downstream processing events. Pre-miRNA is then further processed by the RNase Dicer into mature miRNAs in the cell cytoplasm.[11][16] There also exists an isoform of Drosha that does not contain a nuclear localization signal, which results in the generation of c-Drosha.[17][18] This variant has been shown to localize to the cell cytoplasm rather than the nucleus, but the effects on pri-miRNA processing are yet unclear.

Both Drosha and Dicer also participate in the DNA damage response.[19]

Certain miRNAs have been found to deviate from conventional biogenesis pathways and do not necessarily require Drosha or Dicer, which is because they do not require the processing of pri-miRNA to pre-miRNA.[16] Drosha-independent miRNAs derive from mirtrons, which are genes that encode for miRNAs in their introns and make use of splicing to bypass Drosha cleavage. Simtrons are mirtron-like, splicing-independent, and do require Drosha mediated cleavage, although they do not require most proteins in the canonical pathway such as DGCR8 or Dicer.[10]

Clinical significance

[edit]

Drosha and other miRNA processing enzymes may be important in cancer prognosis.[9] Both Drosha and Dicer can function as master regulators of miRNA processing and have been observed to be down-regulated in some types of breast cancer.[20] The alternative splicing patterns of Drosha in The Cancer Genome Atlas have also indicated that c-drosha appears to be enriched in various types of breast cancer, colon cancer, and esophageal cancer.[18] However, the exact nature of the association between microRNA processing and tumorigenesis is unclear,[21] but its function can be effectively examined by siRNA knockdown based on an independent validation.[22]

Drosha and other miRNA processing enzymes may also be important in HIV-1 replication. miRNAs contribute to the innate antiviral defense. This can be shown by the knockdown of two important miRNA processing proteins, Drosha and Dicer, which leads to a significant enhancement of viral replication in PBMCs from HIV-1-infected patients. Thus, Drosha, in conjunction with Dicer, seem to have a role in controlling HIV-1 replication.[10]

References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000113360 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022191 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Filippov V, Solovyev V, Filippova M, Gill SS (March 2000). "A novel type of RNase III family proteins in eukaryotes". Gene. 245 (1): 213–221. doi:10.1016/s0378-1119(99)00571-5. PMID 10713462.
  6. ^ Filippov V, Solovyev V, Filippova M, Gill SS (March 2000). "A novel type of RNase III family proteins in eukaryotes". Gene. 245 (1): 213–221. doi:10.1016/S0378-1119(99)00571-5. PMID 10713462.
  7. ^ Wu H, Xu H, Miraglia LJ, Crooke ST (November 2000). "Human RNase III is a 160-kDa protein involved in preribosomal RNA processing". The Journal of Biological Chemistry. 275 (47): 36957–36965. doi:10.1074/jbc.M005494200. PMID 10948199.
  8. ^ a b "Entrez Gene: RNASEN ribonuclease III, nuclear".
  9. ^ a b c Slack FJ, Weidhaas JB (December 2008). "MicroRNA in cancer prognosis". The New England Journal of Medicine. 359 (25): 2720–2722. doi:10.1056/NEJMe0808667. PMC 10035200. PMID 19092157.
  10. ^ a b c d Swaminathan G, Navas-Martín S, Martín-García J (March 2014). "MicroRNAs and HIV-1 infection: antiviral activities and beyond". Journal of Molecular Biology. 426 (6): 1178–97. doi:10.1016/j.jmb.2013.12.017. PMID 24370931.
  11. ^ a b c d Lee Y, Ahn C, Han J, Choi H, Kim J, Yim J, et al. (September 2003). "The nuclear RNase III Drosha initiates microRNA processing". Nature. 425 (6956): 415–419. Bibcode:2003Natur.425..415L. doi:10.1038/nature01957. PMID 14508493. S2CID 4421030.
  12. ^ Fortin KR, Nicholson RH, Nicholson AW (August 2002). "Mouse ribonuclease III. cDNA structure, expression analysis, and chromosomal location". BMC Genomics. 3 (1): 26. doi:10.1186/1471-2164-3-26. PMC 122089. PMID 12191433.
  13. ^ Sloan KE, Gleizes PE, Bohnsack MT (May 2016). "Nucleocytoplasmic Transport of RNAs and RNA-Protein Complexes". Journal of Molecular Biology. 428 (10 Pt A): 2040–59. doi:10.1016/j.jmb.2015.09.023. PMID 26434509.
  14. ^ Denli AM, Tops BB, Plasterk RH, Ketting RF, Hannon GJ (November 2004). "Processing of primary microRNAs by the Microprocessor complex". Nature. 432 (7014): 231–235. Bibcode:2004Natur.432..231D. doi:10.1038/nature03049. PMID 15531879. S2CID 4425505.
  15. ^ Han J, Lee Y, Yeom KH, Nam JW, Heo I, Rhee JK, et al. (June 2006). "Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex". Cell. 125 (5): 887–901. doi:10.1016/j.cell.2006.03.043. PMID 16751099. S2CID 453021.
  16. ^ a b c d Suzuki HI, Miyazono K (January 2011). "Emerging complexity of microRNA generation cascades". Journal of Biochemistry. 149 (1): 15–25. doi:10.1093/jb/mvq113. PMID 20876186.
  17. ^ a b Dai L, Chen K, Youngren B, Kulina J, Yang A, Guo Z, et al. (December 2016). "Cytoplasmic Drosha activity generated by alternative splicing". Nucleic Acids Research. 44 (21): 10454–10466. doi:10.1093/nar/gkw668. PMC 5137420. PMID 27471035.
  18. ^ Francia S, Michelini F, Saxena A, Tang D, de Hoon M, Anelli V, et al. (August 2012). "Site-specific DICER and DROSHA RNA products control the DNA-damage response". Nature. 488 (7410): 231–235. Bibcode:2012Natur.488..231F. doi:10.1038/nature11179. PMC 3442236. PMID 22722852.
  19. ^ Thomson JM, Newman M, Parker JS, Morin-Kensicki EM, Wright T, Hammond SM (August 2006). "Extensive post-transcriptional regulation of microRNAs and its implications for cancer". Genes & Development. 20 (16): 2202–2207. doi:10.1101/gad.1444406. PMC 1553203. PMID 16882971.
  20. ^ Iorio MV, Croce CM (June 2012). "microRNA involvement in human cancer". Carcinogenesis. 33 (6): 1126–1133. doi:10.1093/carcin/bgs140. PMC 3514864. PMID 22491715.
  21. ^ Munkácsy G, Sztupinszki Z, Herman P, Bán B, Pénzváltó Z, Szarvas N, et al. (September 2016). "Validation of RNAi Silencing Efficiency Using Gene Array Data shows 18.5% Failure Rate across 429 Independent Experiments". Molecular Therapy. Nucleic Acids. 5 (9): e366. doi:10.1038/mtna.2016.66. PMC 5056990. PMID 27673562.

Further reading

[edit]
[edit]
  • Overview of all the structural information available in the PDB for UniProt: Q9NRR4 (Ribonuclease 3) at the PDBe-KB.
Retrieved from "https://en.wikipedia.org/enwiki/w/index.php?title=Drosha&oldid=1256939625"