Structure of the human sarco/endoplasmic reticulum Ca2+-ATPase 3 gene -: Promoter analysis and alternative splicing of the SERCA3 pre-mRNA

被引:74
作者
Dode, L
De Greef, C
Mountian, I
Attard, M
Town, MM
Casteels, R
Wuytack, F
机构
[1] Katholieke Univ Leuven, Fysiol Lab, B-3000 Louvain, Belgium
[2] Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
关键词
D O I
10.1074/jbc.273.22.13982
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human chromosome 17-specific genomic clones extending over 90 kilobases (kb) of DNA and coding for sarco/endoplasmic reticulum Ca(2+)-ATPase 3 (SERCA3) were isolated. The presence of the D17S1828 genetic marker in the cosmid contig enabled us to map the SERCA3 gene (ATP2A3) 11 centimorgans from the top of the short arm p of chromosome 17, in the vicinity of the cystinosis gene locus. The SERCA3 gene contains 22 exons spread over 50 kb of genomic DNA. The exon/intron boundaries are well conserved between human SERCA3 and SERCA1 genes, except for the junction between exons 8 and 9 which is found in the SERCA1 gene but not in SERCA3 and SERCA2 genes, The transcription start site (+1) is located 152 nucleotides (nt) upstream of the AUG codon, The 5'-flanking region, including exon 1, is embedded in a 1.5-kb CpG island and is characterized by the absence of a TATA box and by the presence of 14 putative Sp1 sites, 11 CACCC boxes, 5 AP-2-binding motifs, 3 GGCTGGGG; motifs, 3 CANNTG boxes, a GATA motif, as well as single sites for Ets-1, c-Myc, and TFIIIc, Functional promoter analysis indicated that the GC-rich region (87% G + C) from -135 to -31 is of critical importance in initiating SERCA3 gene transcription in Jurkat cells. Exon 21 (human, 101 base pairs; mouse, 86 base pairs) can be alternatively excluded, partially included, or totally included, thus generating, respectively, SERCA3a (human and mouse, 999 amino acids (aa)), SERCA3b (human, 1043 aa; mouse, 1038 aa), or SERCA3c (human, 1024 aa; mouse, 1021 aa) isoforms with different C termini, Expression of the mouse SERCA3 isoforms in COS-1 cells demonstrated their ability to function as active pumps, although with different apparent affinities for Ca(2+).
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页码:13982 / 13994
页数:13
相关论文
共 56 条
[51]   LOCALIZATION AND QUANTIFICATION OF ENDOPLASMIC-RETICULUM CA2+-ATPASE ISOFORM TRANSCRIPTS [J].
WU, KD ;
LEE, WS ;
WEY, J ;
BUNGARD, D ;
LYTTON, J .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 269 (03) :C775-C784
[52]   The SERCA3-type of organellar Ca2+ pumps [J].
Wuytack, F ;
Dode, L ;
BabaAissa, F ;
Raeymaekers, L .
BIOSCIENCE REPORTS, 1995, 15 (05) :299-306
[53]  
WUYTACK F, 1994, J BIOL CHEM, V269, P1410
[54]   CA2+-TRANSPORT ATPASES AND THEIR REGULATION IN MUSCLE AND BRAIN [J].
WUYTACK, F ;
RAEYMAEKERS, L ;
DESMEDT, H ;
EGGERMONT, JA ;
MISSIAEN, L ;
VANDENBOSCH, L ;
DEJAEGERE, S ;
VERBOOMEN, H ;
PLESSERS, L ;
CASTEELS, R .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1992, 671 :82-91
[55]  
ZARAINHERZBERG A, 1990, J BIOL CHEM, V265, P4670
[56]   Characterization of cDNA and genomic DNA encoding SERCA1, the Ca2+-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody disease [J].
Zhang, YL ;
Fujii, J ;
Phillips, MS ;
Chen, HS ;
Karpati, G ;
Yee, WC ;
Schrank, B ;
Cornblath, DR ;
Boylan, KB ;
MacLennan, DH .
GENOMICS, 1995, 30 (03) :415-424