A FAMILY OF 3 MOUSE POTASSIUM CHANNEL GENES WITH INTRONLESS CODING REGIONS

被引:151
作者
CHANDY, KG
WILLIAMS, CB
SPENCER, RH
AGUILAR, BA
GHANSHANI, S
TEMPEL, BL
GUTMAN, GA
机构
[1] SEATTLE VET HOSP MED CTR,CTR GERIATR RES EDUC & CLIN,SEATTLE,WA 98108
[2] UNIV CALIF IRVINE,DEPT MICROBIOL & MOLEC GENET,IRVINE,CA 92717
[3] UNIV WASHINGTON,DEPT MED,SEATTLE,WA 98108
[4] UNIV WASHINGTON,DEPT PHARMACOL,SEATTLE,WA 98108
关键词
D O I
10.1126/science.2305265
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To understand the molecular mechanisms responsible for generating physiologically diverse potassium channels in mammalian cells, mouse genomic clones have been isolated with a potassium channel complementary DNA, MBK1, that is homologous to the Drosophila potassium channel gene, Shaker. A family of three closely related potassium channel genes (MKI, MK2, and MK3) that are encoded at distinct genomic loci has been isolated. Sequence analysis reveals that the coding region of each of these three genes exists as a single uninterrupted exon in the mouse genome. This organization precludes the generation of multiple forms of the protein by alternative RNA splicing, a mechanism known to characterize the Drosophila potassium channel genes Shaker and Shab. Thus, mammals may use a different strategy for generating diverse K+ channels by encoding related genes at multiple distinct genomic loci, each of which produces only a single protein.
引用
收藏
页码:973 / 975
页数:3
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