Kawasaki-Nishi Shoko, Yamaguchi Akihito, Forgac Michael, Nishi Tsuyoshi
Department of Cell Membrane Biology, ISIR, Osaka University, 8-1 Mihogaoka, Ibaraki, Osaka, Japan.
Biochem Biophys Res Commun. 2007 Dec 28;364(4):1032-6. doi: 10.1016/j.bbrc.2007.10.118. Epub 2007 Oct 29.
We have identified splicing variants of the mouse a4 subunit which have the same open reading frame but have a different 5'-noncoding sequence. Further determination of the 5'-upstream region of the a4 gene in mouse indicated the presence of two first exons (exon 1a and exon 1b) which include the 5'-noncoding sequence of each variant. The mRNAs of both splicing variants (a4-I and a4-II) show a similar expression pattern in mouse kidney by in situ hybridization. However, tissue and developmental expression patterns of the variants are different. In addition to strong expression in kidney, a4-I expression was detected in heart, lung, skeletal muscle, and testis, whereas a4-II is expressed in lung, liver, and testis. During development, a4-I was expressed beginning with the early embryonic stage, but a4-II mRNA was detected from day 17. These results suggest that each a4 variant has both a tissue and developmental stage specific function.
我们已经鉴定出小鼠α4亚基的剪接变体,它们具有相同的开放阅读框,但5'-非编码序列不同。对小鼠α4基因5'-上游区域的进一步测定表明存在两个第一外显子(外显子1a和外显子1b),它们包含每个变体的5'-非编码序列。通过原位杂交,两种剪接变体(α4-I和α4-II)的mRNA在小鼠肾脏中显示出相似的表达模式。然而,这些变体的组织和发育表达模式是不同的。除了在肾脏中强烈表达外,在心脏、肺、骨骼肌和睾丸中检测到α4-I的表达,而α4-II在肺、肝脏和睾丸中表达。在发育过程中,α4-I从早期胚胎阶段开始表达,但α4-II mRNA在第17天被检测到。这些结果表明每个α4变体都具有组织和发育阶段特异性功能。