Genomic structure of the human CD53 gene
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
8319976
DOI
10.1007/bf00188803
Knihovny.cz E-zdroje
- MeSH
- antigeny CD53 MeSH
- CD antigeny chemie genetika MeSH
- diferenciační antigeny T-lymfocytů chemie genetika MeSH
- genetická transkripce MeSH
- klonování DNA MeSH
- lidé MeSH
- molekulární sekvence - údaje MeSH
- promotorové oblasti (genetika) MeSH
- sekvence aminokyselin MeSH
- sekvence nukleotidů MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny CD53 MeSH
- CD antigeny MeSH
- CD53 protein, human MeSH Prohlížeč
- diferenciační antigeny T-lymfocytů MeSH
The genomic structure of the gene encoding human pan-leukocyte surface glycoprotein CD53 (a member of the "tetraspan family" of membrane proteins) was determined. The gene consists of eight exons encoding all sequences found in cDNA and is spread over more than 26 kilobases of genomic DNA. The exon-intron organization of the CD53 gene is strikingly similar to the CD63 and TAPA-1 genes, which suggests a close evolutionary relationship between these genes. The 5' end of the gene upstream of the first exon contains at least three close transcription start points (approximately 20 base pairs 5' of the 5' end of the published cDNA). The region upstream of the transcription initiation sites is not G+C rich; it contains potential binding sites for several transcriptional factors but no TATA or CCAAT boxes.
Zobrazit více v PubMed
Mol Cell Biol. 1990 Apr;10(4):1680-8 PubMed
Proteins. 1991;9(3):180-90 PubMed
Proc Natl Acad Sci U S A. 1992 Apr 15;89(8):3503-7 PubMed
J Biol Chem. 1991 Jan 5;266(1):117-22 PubMed
Biochem Biophys Res Commun. 1992 May 29;185(1):436-42 PubMed
Mol Cell Biol. 1989 Nov;9(11):5123-33 PubMed
J Immunol. 1990 Oct 1;145(7):2207-13 PubMed
J Exp Med. 1991 Dec 1;174(6):1347-54 PubMed
Blood. 1992 Feb 15;79(4):865-70 PubMed
Cell. 1990 Apr 6;61(1):113-24 PubMed
J Immunol. 1990 Dec 15;145(12):4322-5 PubMed
FEBS Lett. 1991 Aug 19;288(1-2):1-4 PubMed
J Immunol. 1991 Aug 1;147(3):1030-6 PubMed
Mol Cell Biol. 1991 May;11(5):2864-72 PubMed
Eur J Immunol. 1991 Feb;21(2):377-83 PubMed
Gene. 1987;57(2-3):229-37 PubMed
J Biol Chem. 1991 Feb 15;266(5):3239-45 PubMed
J Biol Chem. 1989 Jul 25;264(21):12289-93 PubMed
Cell. 1989 Apr 7;57(1):103-13 PubMed
Mol Cell Biol. 1990 Aug;10(8):4007-15 PubMed
J Biol Chem. 1991 Jan 25;266(3):1903-9 PubMed
Immunogenetics. 1990;32(4):281-5 PubMed
Blood. 1991 Jul 15;78(2):280-4 PubMed
J Virol. 1989 May;63(5):1924-8 PubMed
Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7 PubMed
Proc Natl Acad Sci U S A. 1991 Jan 15;88(2):603-7 PubMed
Science. 1989 Jul 28;245(4916):371-8 PubMed
J Mol Biol. 1990 Oct 5;215(3):403-10 PubMed
J Immunol. 1990 Apr 15;144(8):3195-200 PubMed
Blood. 1992 Feb 1;79(3):602-9 PubMed
Mol Cell Biol. 1992 Jun;12 (6):2662-72 PubMed
Immunogenetics. 1993;37(6):461-5 PubMed
J Immunol. 1992 Nov 1;149(9):2879-86 PubMed
Mol Cell Biol. 1991 Mar;11(3):1614-23 PubMed
Proc Natl Acad Sci U S A. 1990 Sep;87(17):6833-7 PubMed
Nucleic Acids Res. 1987 Sep 11;15(17):7155-74 PubMed
J Exp Med. 1992 Feb 1;175(2):527-36 PubMed
J Immunol. 1985 Sep;135(3):1987-97 PubMed
Anal Biochem. 1987 Apr;162(1):156-9 PubMed
Science. 1989 Nov 10;246(4931):780-6 PubMed
Nucleic Acids Res. 1990 May 11;18(9):2793-9 PubMed
J Exp Med. 1989 Apr 1;169(4):1497-502 PubMed
Comput Appl Biosci. 1991 Apr;7(2):203-6 PubMed
J Immunol. 1992 May 1;148(9):2826-33 PubMed
Mol Cell Biol. 1991 Oct;11(10):5338-45 PubMed
GENBANK
L11670, L11671
