Serinski inkorporator 3 jest protein koji je kod ljudi kodiran genom SERINC3.[5][6] Demonstrirano je da se SERINC3 ponaša kao faktor restrikcije retrovirusa.[7][8][9]

SERINC3
Identifikatori
AliasiSERINC3
Vanjski ID-jeviOMIM: 607165 MGI: 1349457 HomoloGene: 38230 GeneCards: SERINC3
Lokacija gena (čovjek)
Hromosom 20 (čovjek)
Hrom.Hromosom 20 (čovjek)[1]
Hromosom 20 (čovjek)
Genomska lokacija za SERINC3
Genomska lokacija za SERINC3
Bend20q13.12Početak44,496,221 bp[1]
Kraj44,522,085 bp[1]
Lokacija gena (miš)
Hromosom 2 (miš)
Hrom.Hromosom 2 (miš)[2]
Hromosom 2 (miš)
Genomska lokacija za SERINC3
Genomska lokacija za SERINC3
Bend2|2 H3Početak163,465,192 bp[2]
Kraj163,487,051 bp[2]
Obrazac RNK ekspresije




Više referentnih podataka o ekspresiji
Ontologija gena
Molekularna funkcija L-serine transmembrane transporter activity
Ćelijska komponenta integral component of membrane
Golđijeva membrana
Golđijev aparat
membrana
citoplazma
perinuklearno područje citoplazme
ćelijska membrana
Biološki proces phosphatidylserine metabolic process
detection of virus
Urođeni imunski sistem
defense response to virus
positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway
sphingolipid metabolic process
L-serine transport
immune system process
L-serine biosynthetic process
Izvori:Amigo / QuickGO
Ortolozi
VrsteČovjekMiš
Entrez
Ensembl
UniProt
RefSeq (mRNK)

NM_198941
NM_006811

NM_012032

RefSeq (bjelančevina)

NP_006802
NP_945179

NP_036162

Lokacija (UCSC)Chr 20: 44.5 – 44.52 MbChr 2: 163.47 – 163.49 Mb
PubMed pretraga[3][4]
Wikipodaci
Pogledaj/uredi – čovjekPogledaj/uredi – miš

Model organizmi uredi

U proučavanju funkcije SERINC3 upotrebljavani su u modwelni organizmi. Uvjetna linijas nokaut miša zvana Serinc3tm1a(KOMP)Wtsi generirana je u Wellcome Trust Sanger Institute.[10] Muške i ženske životinje prolazile su standardizirani fenotipski skrining[11] za određivanje efekata delecije.[12][13][14][15] Izvršeni dodatni snimcii: - Dubinsko imunsko fenotipiziranje[16]

Fenotip Serinc3 nokaut-miša
Svojstvo Fenotip
Svi podaci raspoloživi su na linku.[11][16]
Insulin Normalan
Vijabilnost homozigota na P14 Normalna
Plodnost homozigota Normalna
Tjelesna težina Normalna
Neurološka procjena Normalna
Snaga stiska Normalna
Dismorfologija Normalna
Indirektana kalorimetrija Normalna
Test tolerancije glukoze Normalan
Slušni odgovor moždanog debla Normalan
DEXA Normalna
Radiografija Normalna
Morfologija oka Normalna
Klinička hemija Normalna
Hematologija 16 sedmica Normal
Leukociti periferne krvi 16 sedmica Normalni
Težina srca Normalna
Salmonella infekcija Normalna
Imunofenotipizacija slezene Normalna
Imunofenotipizacija mezenternih limfnih čvorova Normalna
Epidermni imunski sastav Normalan
Izazov gripe Normalan

Reference uredi

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000132824 - Ensembl, maj 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000017707 - Ensembl, maj 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. ^ Bossolasco M, Lebel M, Lemieux N, Mes-Masson AM (novembar 1999). "The human TDE gene homologue: localization to 20q13.1-13.3 and variable expression in human tumor cell lines and tissue". Molecular Carcinogenesis. 26 (3): 189–200. doi:10.1002/(SICI)1098-2744(199911)26:3<189::AID-MC8>3.0.CO;2-T. PMID 10559794.
  6. ^ "Entrez Gene: SERINC3 serine incorporator 3".
  7. ^ Rosa A, Chande A, Ziglio S, De Sanctis V, Bertorelli R, Goh SL, et al. (oktobar 2015). "HIV-1 Nef promotes infection by excluding SERINC5 from virion incorporation". Nature. 526 (7572): 212–7. doi:10.1038/nature15399. PMC 4861059. PMID 26416734.
  8. ^ Chande A, Cuccurullo EC, Rosa A, Ziglio S, Carpenter S, Pizzato M (novembar 2016). "S2 from equine infectious anemia virus is an infectivity factor which counteracts the retroviral inhibitors SERINC5 and SERINC3". Proceedings of the National Academy of Sciences of the United States of America. 113 (46): 13197–13202. doi:10.1073/pnas.1612044113. PMC 5135340. PMID 27803322.
  9. ^ Ramdas, Pavitra; Bhardwaj, Vipin; Singh, Aman; Vijay, Nagarjun; Chande, Ajit (24. 2. 2020). "Coevolution of retroviruses with SERINCs following whole-genome duplication divergence". bioRxiv. doi:10.1101/2020.02.24.962506.
  10. ^ Gerdin AK (2010). "The Sanger Mouse Genetics Programme: high throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x. S2CID 85911512.
  11. ^ a b "International Mouse Phenotyping Consortium".
  12. ^ Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, et al. (juni 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
  13. ^ Dolgin E (juni 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  14. ^ Collins FS, Rossant J, Wurst W (januar 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. S2CID 18872015.
  15. ^ White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, et al. (juli 2013). "Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes". Cell. 154 (2): 452–64. doi:10.1016/j.cell.2013.06.022. PMC 3717207. PMID 23870131.
  16. ^ a b "Infection and Immunity Immunophenotyping (3i) Consortium".[mrtav link]

Dopunska literatura uredi