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小鼠蛋白磷酸酶1cγ(Ppp1cc)基因的基因组结构与功能分析

Genomic organization and functional analysis of the murine protein phosphatase 1c gamma (Ppp1cc) gene.

作者信息

Okano K, Heng H, Trevisanato S, Tyers M, Varmuza S

机构信息

Department of Zoology, University of Toronto, Ontario, Canada.

出版信息

Genomics. 1997 Oct 1;45(1):211-5. doi: 10.1006/geno.1997.4907.

Abstract

Protein phosphatase 1 holoenzymes are composed of catalytic subunits in combination with various regulatory subunits. In rodents, four different catalytic isoforms are known, PP1c alpha, -delta, -gamma 1, and -gamma 2. Here we describe the genomic organization of the murine Ppp1cc gene that encodes the PP1c gamma 1 and PP1c gamma 2 isoforms. We determined that Ppp1cc maps to F1.2-G1.2 on chromosome 5 by FISH mapping. Southern hybridization and analysis of cross-hybridizing genomic clones revealed four Ppp1cc-related pseudogenes in the mouse genome. The authentic Ppp1cc gene encodes two isoforms, PP1c gamma 1 and PP1c gamma 2, that arise from alternative splicing and differ by retention of the last intron. The introns of Ppp1cc are flanked by short direct repeats, the significance of which is not clear. Both isoforms retain phosphatase function since they are able to complement the cold-sensitive PP1 defect caused by the dis2-11 mutation in the fission yeast Schizosaccharomyces pombe.

摘要

蛋白磷酸酶1全酶由催化亚基与各种调节亚基结合组成。在啮齿动物中,已知有四种不同的催化同工型,即PP1cα、-δ、-γ1和-γ2。在此,我们描述了编码PP1cγ1和PP1cγ2同工型的小鼠Ppp1cc基因的基因组结构。我们通过荧光原位杂交定位确定Ppp1cc定位于5号染色体上的F1.2 - G1.2。Southern杂交和对交叉杂交基因组克隆的分析揭示了小鼠基因组中有四个与Ppp1cc相关的假基因。真正的Ppp1cc基因编码两种同工型,PP1cγ1和PP1cγ2,它们通过可变剪接产生,区别在于最后一个内含子的保留。Ppp1cc的内含子两侧是短的直接重复序列,其意义尚不清楚。两种同工型都保留了磷酸酶功能,因为它们能够弥补裂殖酵母粟酒裂殖酵母中dis2 - 11突变引起的冷敏感PP1缺陷。

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