Escalante R, Sastre L
Instituto de Investigaciones Biomédicas del CSIC, Madrid, Spain.
DNA Cell Biol. 1995 Oct;14(10):893-900. doi: 10.1089/dna.1995.14.893.
The sarco/endoplasmic reticulum Ca-ATPase gene from Artemia franciscana is transcribed into two mRNAs of 4.5 and 5.2 kb that code for protein isoforms differing at their carboxyl terminus. Northern blot assays and anchored polymerase chain reaction (PCR) experiments have shown that these two mRNAs also differ at the initial part of their 5' untranslated region. The 5.2-kb mRNA-specific 5' untranslated region is present as an independent exon whose transcription is regulated by a promoter different from the one previously described that regulates the expression of the 4.5-kb mRNA. The nucleotide sequence of the 5.2-kb mRNA promoter and the transcription initiation site have been determined. These results suggest that the expression of the two protein isoforms is regulated in A. franciscana at the transcription initiation step, in contrast with the vertebrates sarco/endoplasmic reticulum Ca-ATPase genes 1 and 2 which have unique promoters for transcription of the two isoforms encoded by each gene.
来自卤虫的肌浆/内质网Ca - ATP酶基因转录成4.5 kb和5.2 kb的两种mRNA,它们编码的蛋白质异构体在羧基末端存在差异。Northern印迹分析和锚定聚合酶链反应(PCR)实验表明,这两种mRNA在其5'非翻译区的起始部分也存在差异。5.2 kb mRNA特异的5'非翻译区作为一个独立的外显子存在,其转录受一个与先前描述的调控4.5 kb mRNA表达的启动子不同的启动子调控。已确定了5.2 kb mRNA启动子的核苷酸序列和转录起始位点。这些结果表明,与脊椎动物的肌浆/内质网Ca - ATP酶基因1和2不同,卤虫中两种蛋白质异构体的表达在转录起始步骤受到调控,脊椎动物的这两个基因各自具有独特的启动子来转录所编码的两种异构体。