Jump to content

LMAN1: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
addition of more recent ref, link to ERGIC and link to an open figure that demonstrates the pathway
m fix citations
Line 25: Line 25:
*{{cite journal |vauthors=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, etal |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library |journal=Gene |volume=200 |issue= 1–2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 }}
*{{cite journal |vauthors=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, etal |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library |journal=Gene |volume=200 |issue= 1–2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 }}
*{{cite journal |vauthors=Nichols WC, Terry VH, Wheatley MA, etal |title=ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families |journal=Blood |volume=93 |issue= 7 |pages= 2261–6 |year= 1999 |pmid= 10090935 |doi= }}
*{{cite journal |vauthors=Nichols WC, Terry VH, Wheatley MA, etal |title=ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families |journal=Blood |volume=93 |issue= 7 |pages= 2261–6 |year= 1999 |pmid= 10090935 |doi= }}
*{{cite journal |vauthors=Saifuddin M, Hart ML, Gewurz H, etal |title=Interaction of mannose-binding lectin with primary isolates of human immunodeficiency virus type 1 |journal=J. Gen. Virol. |volume=81 |issue= Pt 4 |pages= 949–55 |year= 2000 |pmid= 10725420 |doi= }}
*{{cite journal |vauthors=Saifuddin M, Hart ML, Gewurz H, etal |title=Interaction of mannose-binding lectin with primary isolates of human immunodeficiency virus type 1 |journal=J. Gen. Virol. |volume=81 |issue= Pt 4 |pages= 949–55 |year= 2000 |pmid= 10725420 |doi= 10.1099/0022-1317-81-4-949}}
*{{cite journal |vauthors=Harris RA, Yang A, Stein RC, etal |title=Cluster analysis of an extensive human breast cancer cell line protein expression map database |journal=Proteomics |volume=2 |issue= 2 |pages= 212–23 |year= 2002 |pmid= 11840567 |doi=10.1002/1615-9861(200202)2:2<212::AID-PROT212>3.0.CO;2-H }}
*{{cite journal |vauthors=Harris RA, Yang A, Stein RC, etal |title=Cluster analysis of an extensive human breast cancer cell line protein expression map database |journal=Proteomics |volume=2 |issue= 2 |pages= 212–23 |year= 2002 |pmid= 11840567 |doi=10.1002/1615-9861(200202)2:2<212::AID-PROT212>3.0.CO;2-H }}
*{{cite journal |vauthors=Jüliger S, Kremsner PG, Alpers MP, etal |title=Restricted polymorphisms of the mannose-binding lectin gene in a population of Papua New Guinea |journal=Mutat. Res. |volume=505 |issue= 1–2 |pages= 87–91 |year= 2002 |pmid= 12175909 |doi=10.1016/S0027-5107(02)00142-2 }}
*{{cite journal |vauthors=Jüliger S, Kremsner PG, Alpers MP, etal |title=Restricted polymorphisms of the mannose-binding lectin gene in a population of Papua New Guinea |journal=Mutat. Res. |volume=505 |issue= 1–2 |pages= 87–91 |year= 2002 |pmid= 12175909 |doi=10.1016/S0027-5107(02)00142-2 }}

Revision as of 02:42, 20 August 2017

LMAN1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLMAN1, ERGIC-53, ERGIC53, F5F8D, FMFD1, MCFD1, MR60, gp58, lectin, mannose binding 1
External IDsOMIM: 601567; MGI: 1917611; HomoloGene: 4070; GeneCards: LMAN1; OMA:LMAN1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005570

NM_001172062
NM_027400

RefSeq (protein)

NP_005561

NP_001165533
NP_081676

Location (UCSC)Chr 18: 59.33 – 59.36 MbChr 18: 66.11 – 66.16 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Protein ERGIC-53 also known as ER-Golgi intermediate compartment 53 kDa protein or lectin mannose-binding 1 is a protein that in humans is encoded by the LMAN1 gene.[5][6][7]

Function

ERGIC-53 (also named LMAN1) is a type I integral membrane protein localized in the intermediate region (ERGIC) between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined deficiency of factor V-factor VIII, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.[8][7] MCFD2 is the second gene that leads to combined deficiency of factor V-factor VIII.[9] ERGIC-53 and MCFD2 form a protein complex and serve as a cargo receptor to transport FV and FVIII from the ER to the ERGIC and then the Golgi,[10]as illustrated here.[8]

Clinical significance

LMAN1 mutational inactivation is a frequent and early event potentially contributing to colorectal tumorigenesis.[11]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000074695Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000041891Ensembl, 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. ^ Nichols WC, Seligsohn U, Zivelin A, Terry VH, Hertel CE, Wheatley MA, Moussalli MJ, Hauri HP, Ciavarella N, Kaufman RJ, Ginsburg D (May 1998). "Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII". Cell. 93 (1): 61–70. doi:10.1016/S0092-8674(00)81146-0. PMID 9546392.
  6. ^ Arar C, Mignon C, Mattei M, Monsigny M, Roche A, Legrand A (Feb 1997). "Mapping of the MR60/ERGIC-53 gene to human chromosome 18q21.3-18q22 by in situ hybridization". Mamm Genome. 7 (10): 791–2. doi:10.1007/s003359900238. PMID 8854877.
  7. ^ a b "Entrez Gene: LMAN1 lectin, mannose-binding, 1".
  8. ^ a b Khoriaty R, Vasievich MP, Ginsburg D., Blood. 2012 Jul 5;120(1):31-8. doi: 10.1182/blood-2012-01-292086. "The COPII pathway and hematologic disease". www.bloodjournal.org. American Society of Hematology. Retrieved 7 April 2017.{{cite web}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  9. ^ Zhang B, Cunningham MA, Nichols WC, Bernat JA, Seligsohn U, Pipe SW, McVey JH, Schulte-Overberg U, de Bosch NB, Ruiz-Saez A, White GC, Tuddenham EG, Kaufman RJ, Ginsburg D (May 2003). "Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex". Nat Genet. 34 (2): 220–5. doi:10.1038/ng1153. PMID 12717434.
  10. ^ Zhang B, Kaufman RJ, Ginsburg D (2005). "LMAN1 and MCFD2 form a cargo receptor complex and interact with coagulation factor VIII in the early secretory pathway". J. Biol. Chem. 280 (27): 25881–6. doi:10.1074/jbc.M502160200. PMID 15886209.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  11. ^ Roeckel N, Woerner SM, Kloor M, Yuan YP, Patsos G, Gromes R, Kopitz J, Gebert J (January 2009). "High frequency of LMAN1 abnormalities in colorectal tumors with microsatellite instability". Cancer Res. 69 (1): 292–9. doi:10.1158/0008-5472.CAN-08-3314. PMID 19118014.

Further reading