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{{Rfam_box|acc=RNA_secondary_structure_and_sequence_conservation_for_miR-96| description=mir-96 microRNA precursor family |abbreviation=mir-96 | avg_length=77.6 |avg_identity=79 |type=Gene; miRNA; |se=miRBase; Wilkinson A |ss=Predicted; WAR |release=9.1}}
{{Rfam_box|acc=RNA_secondary_structure_and_sequence_conservation_for_miR-96| description=mir-96 microRNA precursor family |abbreviation=mir-96 | avg_length=77.6 |avg_identity=79 |type=Gene; miRNA; |se=miRBase; Wilkinson A |ss=Predicted; WAR |release=9.1}}


__TOC__
{{PBB|geneid=407053}}

⚫
[[Image:MiR-96_sequence_alignment.png|thumb|left|400px|A multiple sequence alignment of precursor miR-96 molecules. Highly conserved nucleotides are coloured in red, less well conserved nucleotides are coloured orange and non-conserved nucleotides are coloured blue or white. The columns corresponding to the mature and seed sequence are indicated above the alignment. The canonical human sequence and the two human variant sequences that are implicated in hearing loss (13G>A and 14C>A) are in the first, second and third rows respectively.]]


'''miR-96 microRNA precursor''' is a small [[non-coding RNA]] that regulates [[gene expression]]. [[microRNAs]] are transcribed as ~80 [[nucleotide]] precursors and subsequently processed by the [[Dicer]] enzyme to give a ~23 nucleotide products. In this case the mature sequence comes from the 5' arm of the precursor.
'''miR-96 microRNA precursor''' is a small [[non-coding RNA]] that regulates [[gene expression]]. [[microRNAs]] are transcribed as ~80 [[nucleotide]] precursors and subsequently processed by the [[Dicer]] enzyme to give a ~23 nucleotide products. In this case the mature sequence comes from the 5' arm of the precursor.
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<ref name="pmid14534255">{{cite journal |author=Goodyear RJ, Legan PK, Wright MB, Marcotti W, Oganesian A, Coats SA, Booth CJ, Kros CJ, Seifert RA, Bowen-Pope DF, Richardson GP |title=A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles. |journal=J Neurosci |volume=23 |issue=27 |pages=9208–19 |year=2003 |pmid=14534255}}</ref>
<ref name="pmid14534255">{{cite journal |author=Goodyear RJ, Legan PK, Wright MB, Marcotti W, Oganesian A, Coats SA, Booth CJ, Kros CJ, Seifert RA, Bowen-Pope DF, Richardson GP |title=A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles. |journal=J Neurosci |volume=23 |issue=27 |pages=9208–19 |year=2003 |pmid=14534255}}</ref>
<ref name="pmid12441305">{{cite journal |author=Wallis D, Hamblen M, Zhou Y, Venken KJ, Schumacher A, Grimes HL, Zoghbi HY, Orkin SH, Bellen HJ |title=The zinc finger transcription factor Gfi1, implicated in lymphomagenesis, is required for inner ear hair cell differentiation and survival. |journal=Development |volume=130 |issue=1 |pages=221–32 |year=2003 |pmid=12441305}}</ref>
<ref name="pmid12441305">{{cite journal |author=Wallis D, Hamblen M, Zhou Y, Venken KJ, Schumacher A, Grimes HL, Zoghbi HY, Orkin SH, Bellen HJ |title=The zinc finger transcription factor Gfi1, implicated in lymphomagenesis, is required for inner ear hair cell differentiation and survival. |journal=Development |volume=130 |issue=1 |pages=221–32 |year=2003 |pmid=12441305}}</ref>

⚫
[[Image:MiR-96_sequence_alignment.png|thumb|center|600px|A multiple sequence alignment of precursor miR-96 molecules. Highly conserved nucleotides are coloured in red, less well conserved nucleotides are coloured orange and non-conserved nucleotides are coloured blue or white. The columns corresponding to the mature and seed sequence are indicated above the alignment. The canonical human sequence and the two human variant sequences that are implicated in hearing loss (13G>A and 14C>A) are in the first, second and third rows respectively.]]

{{-}}


==References==
==References==

Revision as of 13:38, 3 August 2010

Mir-96 microRNA
Identifiers
Other data
PDB structuresPDBe

miR-96 microRNA precursor is a small non-coding RNA that regulates gene expression. microRNAs are transcribed as ~80 nucleotide precursors and subsequently processed by the Dicer enzyme to give a ~23 nucleotide products. In this case the mature sequence comes from the 5' arm of the precursor. [1] The mature products are thought to have regulatory roles through complementarity to mRNA. These microRNAs are expressed specifically in the inner ear and the adult eye.[2][3]

miR-96 is thought to be conserved within Nephrozoa, i.e. the Deuterostomes and Protostomes. [4]

Variation within the seed region of mature miR-96 has been associated with autosomal dominant, progressive hearing loss in humans and mice. The homozygous mutant mice were profoundly deaf, showing no cochlear responses. Heterozygous mice and humans progressively lose the ability to hear. [5] [6] [7] Five genes, of 132 predicted targets, have been experimentally validated as targets of miR-96: Aqp5, Celsr2, Myrip, Odf2 and Ryk.[6]

Microarray analysis of 4-day old wildtype and mutant mice showed that in the 3' UTR of upregulated genes, there was a significant enrichment in heptamers complementary to miR-96, implying that miR-96 normally affects a wide range of target genes, and that the mutation results in a loss of normal targets. Among the downregulated genes, there is a significant enrichment in heptamers complementary to the mutant miR-96, so the mutant miR-96 has gained novel targets.[6] Among the downregulated genes were five of particular interest; Ocm, Pitpnm1, Prestin, Ptprq and Gfi1, all of which are strongly and specifically expressed in hair cells. Mice mutant for the latter three exhibit deafness and hair cell degeneration. [8] [9] [10]

A multiple sequence alignment of precursor miR-96 molecules. Highly conserved nucleotides are coloured in red, less well conserved nucleotides are coloured orange and non-conserved nucleotides are coloured blue or white. The columns corresponding to the mature and seed sequence are indicated above the alignment. The canonical human sequence and the two human variant sequences that are implicated in hearing loss (13G>A and 14C>A) are in the first, second and third rows respectively.

References

  1. ^ Mourelatos Z, Dostie J, Paushkin S, Sharma A, Charroux B, Abel L, Rappsilber J, Mann M, Dreyfuss G (2002). "miRNPs: a novel class of ribonucleoproteins containing numerous microRNAs". Genes Dev. 16 (6): 720–8. doi:10.1101/gad.974702. PMC 155365. PMID 11914277.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^ Weston MD, Pierce ML, Rocha-Sanchez S, Beisel KW, Soukup GA (2006). "MicroRNA gene expression in the mouse inner ear". Brain Res. 1111 (1): 95–104. doi:10.1016/j.brainres.2006.07.006. PMID 16904081.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ Xu S, Witmer PD, Lumayag S, Kovacs B, Valle D (2007). "MicroRNA (miRNA) transcriptome of mouse retina and identification of a sensory organ-specific miRNA cluster". J Biol Chem. 282 (34): 25053–66. doi:10.1074/jbc.M700501200. PMID 17597072.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
  4. ^ Wheeler BM, Heimberg AM, Moy VN, Sperling EA, Holstein TW, Heber S, Peterson KJ (2009). "The deep evolution of metazoan microRNAs". Evol Dev. 11 (1): 50–68. doi:10.1111/j.1525-142X.2008.00302.x. PMID 19196333.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ Mencía A, Modamio-Høybjør S, Redshaw N, Morín M, Mayo-Merino F, Olavarrieta L, Aguirre LA, del Castillo I, Steel KP, Dalmay T, Moreno F, Moreno-Pelayo MA (2009). "Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss". Nat Genet. 41 (5): 609–13. doi:10.1038/ng.355. PMID 19363479.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ a b c Lewis MA, Quint E, Glazier AM, Fuchs H, De Angelis MH, Langford C, van Dongen S, Abreu-Goodger C, Piipari M, Redshaw N, Dalmay T, Moreno-Pelayo MA, Enright AJ, Steel KP (2009). "An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice". Nat Genet. 41 (5): 614–8. doi:10.1038/ng.369. PMC 2705913. PMID 19363478.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  7. ^ Soukup GA (2009). "Little but loud: Small RNAs have a resounding affect on ear development". Brain Res. 1277: 104–14. doi:10.1016/j.brainres.2009.02.027. PMC 2700218. PMID 19245798.
  8. ^ Liberman MC, Gao J, He DZ, Wu X, Jia S, Zuo J (2002). "Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier". Nature. 419 (6904): 300–4. doi:10.1038/nature01059. PMID 12239568.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  9. ^ Goodyear RJ, Legan PK, Wright MB, Marcotti W, Oganesian A, Coats SA, Booth CJ, Kros CJ, Seifert RA, Bowen-Pope DF, Richardson GP (2003). "A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles". J Neurosci. 23 (27): 9208–19. PMID 14534255.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. ^ Wallis D, Hamblen M, Zhou Y, Venken KJ, Schumacher A, Grimes HL, Zoghbi HY, Orkin SH, Bellen HJ (2003). "The zinc finger transcription factor Gfi1, implicated in lymphomagenesis, is required for inner ear hair cell differentiation and survival". Development. 130 (1): 221–32. PMID 12441305.{{cite journal}}: CS1 maint: multiple names: authors list (link)

Media reports

Further reading

  • Kondkar AA, Bray MS, Leal SM; et al. (2010). "VAMP8/endobrevin is overexpressed in hyperreactive human platelets: suggested role for platelet microRNA". J. Thromb. Haemost. 8 (2): 369–78. doi:10.1111/j.1538-7836.2009.03700.x. PMID 19943878. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  • Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A; et al. (2004). "A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci". J. Med. Genet. 41 (2): e14. PMID 14757864. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  • Guttilla IK, White BA (2009). "Coordinate regulation of FOXO1 by miR-27a, miR-96, and miR-182 in breast cancer cells". J. Biol. Chem. 284 (35): 23204–16. doi:10.1074/jbc.M109.031427. PMID 19574223.{{cite journal}}: CS1 maint: unflagged free DOI (link)
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