Wymore R S, Negulescu D, Kinoshita K, Kalman K, Aiyar J, Gutman G A, Chandy K G
Department of Physiology, University of California, Irvine, California 92717, USA.
J Biol Chem. 1996 Jun 28;271(26):15629-34. doi: 10.1074/jbc.271.26.15629.
The mouse voltage-gated K+ channel gene, Kv1.4, is expressed in brain and heart as approximately 4.5- and approximately 3.5-kilobase (kb) transcripts. Both mRNAs begin at a common site 1338 bp upstream of the initiation codon, contain 3477 and 4411 nucleotides, respectively, and are encoded by two exons; exon 1 contains 0.5 kb of the 5'-noncoding region (NCR), while exon 2 encodes the remaining 0.8 kb of the 5'-NCR, the entire coding region (2 kb), and all of the 3'-NCR. The 3.5-kb transcript terminates at a polyadenylation signal 177 bp 3' of the stop codon, while the 4.5-kb mRNA utilizes a signal 94 bp farther downstream. Although the proteins generated from either transcript are identical, the two mRNAs are functionally different, the 3.5-kb transcript producing approximately 4-5-fold larger currents when expressed in Xenopus oocytes compared to the 4. 5-kb mRNA. The decreased expression of the longer transcript is due to the presence of five ATTTA repeats in the 3'-NCR which inhibit translation; such motifs have also been reported to destabilize the messages of many other genes and might therefore shorten the life of the 4.5-kb transcript during its natural expression. The Kv1.4 basal promoter is GC-rich, contains three SP1 repeats (CCGCCC, -65 to -35), lacks canonical TATAAA and GGCAATCT motifs, and has no apparent tissue specificity. One region enhances activity of this promoter. Thus, transcriptional and post-transcriptional regulation of mKv1.4, coupled with selective usage of the two alternate Kv1.4 mRNAs, may modulate the levels of functional Kv1.4 channels.
小鼠电压门控钾离子通道基因Kv1.4在脑和心脏中表达,其转录本大小约为4.5千碱基(kb)和3.5千碱基。这两种mRNA均起始于起始密码子上游1338 bp处的一个共同位点,分别包含3477和4411个核苷酸,由两个外显子编码;外显子1包含5'非编码区(NCR)的0.5 kb,而外显子2编码5'NCR的其余0.8 kb、整个编码区(2 kb)以及所有3'NCR。3.5 kb的转录本在终止密码子下游177 bp处的多聚腺苷酸化信号处终止,而4.5 kb的mRNA则利用更下游94 bp处的信号。尽管由任一转录本产生的蛋白质是相同的,但这两种mRNA在功能上有所不同,与4.5 kb的mRNA相比,3.5 kb的转录本在非洲爪蟾卵母细胞中表达时产生的电流大约大4 - 5倍。较长转录本表达量的降低是由于3'NCR中存在五个ATTTA重复序列,它们抑制翻译;据报道,这样的基序也会使许多其他基因的信使RNA不稳定,因此可能会缩短4.5 kb转录本在自然表达过程中的寿命。Kv1.4基础启动子富含GC,包含三个SP1重复序列(CCGCCC,-65至-35),缺乏典型的TATAAA和GGCAATCT基序,且没有明显的组织特异性。有一个区域可增强该启动子的活性。因此,mKv1.4的转录和转录后调控,再加上对两种交替的Kv1.4 mRNA的选择性使用,可能会调节功能性Kv1.4通道的水平。