A new splicing acceptor site and poly(A)+ sequence signal within DQA1*0401 and DQA1*0501 mRNA 3′UTR contribute to increase the extraordinary diversity of mRNA isoforms

Immunogenetics

Volumn 57, Issue 3-4, 2005, Pages 182-188

  Hoarau, J J ^a   Festy, F ^b   Cesari, M ^b   Pabion, M ^c  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b UNIVERSITÉ DE LA RÉUNION   (France)

^c INSTITUT ALBERT BONNIOT   (France)

Author keywords

3 UTR; DQA1 gene; Polyadenylation; Post transcriptional regulation; Splicing

Indexed keywords

HLA DQA1 ANTIGEN; MESSENGER RNA; POLYADENYLIC ACID;

3' UNTRANSLATED REGION; ALLELE; ARTICLE; B LYMPHOBLAST; BINDING SITE; CELL LINE; CONTROLLED STUDY; GENE SEQUENCE; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; NUCLEOTIDE SEQUENCE; POLYADENYLATION; PRIORITY JOURNAL; RNA SPLICING;

3' UNTRANSLATED REGIONS; B-LYMPHOCYTES; BASE SEQUENCE; BINDING SITES; CELL LINE; DNA, COMPLEMENTARY; HLA-DQ ANTIGENS; HUMANS; MOLECULAR SEQUENCE DATA; RNA SPLICING; RNA, MESSENGER; SEQUENCE HOMOLOGY, NUCLEIC ACID; SIGNAL TRANSDUCTION; VARIATION (GENETICS);

EID: 20144373315     PISSN: 00937711     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00251-005-0769-3     Document Type: Article

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