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肿瘤抑制因子 Stk11 基因在小鼠中差异表达的新型选择性剪接转录变体。

Differentially expressed novel alternatively spliced transcript variant of tumor suppressor Stk11 gene in mouse.

机构信息

Department of Biochemistry, Faculty of Life Sciences, A.M. University, Aligarh, UP 202002, India.

Department of Biosciences, Jamia Millia Islamia, New Delhi, 110025, India.

出版信息

Gene. 2018 Aug 20;668:146-154. doi: 10.1016/j.gene.2018.05.053. Epub 2018 May 17.

DOI:10.1016/j.gene.2018.05.053
PMID:29777910
Abstract

Serine/threonine kinase 11 (STK11) is a protein kinase that is encoded by Stk11 gene located on chromosome 19 and 10 in humans and mouse respectively. It acts as a master kinase of adenine monophosphate-activated protein kinase (AMPK) pathway that coordinates the regulation of cellular energy metabolism and cell division. STK11 exerts effect by activating more than 14 kinases including AMPK and AMPK-related kinases. It is also known to regulate cell polarity and acts as tumor suppressor. Alternative splicing of pre-mRNA is a mechanism which results in multiple transcript variants of a single gene. In human, two STK11 isoforms have been reported, an alternatively spliced isoform which has variation at its C-terminal and mostly expressed in testis (LKB1). Another isoform exhibiting oncogenic properties lacks few residues at its N-terminal (ΔN-LKB1). In the present study, we report the identification of a new transcript variant Stk11N which is generated through alternative splicing. The new variant was found to have differential and tissue specific expression at Postnatal-7 and adult stages of mouse. As compared to the known variant Stk11C, the conceptually translated amino acid sequences of the new variant differ from exon-E2 onwards. In silico post translational studies of the new and published variant show similarity in some of the properties while differ in properties like nuclear export signals, phosphorylation, glycosylation, etc. Thus, alternative splicing of Stk11 gene generating new variant with heterogeneous properties suggests for complex regulation of these variants in controlling the AMPK pathway and other functions.

摘要

丝氨酸/苏氨酸激酶 11(STK11)是一种蛋白激酶,由 Stk11 基因编码,该基因分别位于人类和小鼠的 19 号和 10 号染色体上。它作为腺嘌呤单磷酸激活蛋白激酶(AMPK)通路的主激酶,协调细胞能量代谢和细胞分裂的调节。STK11 通过激活超过 14 种激酶(包括 AMPK 和 AMPK 相关激酶)发挥作用。它还已知调节细胞极性并作为肿瘤抑制因子发挥作用。前体 mRNA 的选择性剪接是一种导致单个基因的多个转录变体的机制。在人类中,已经报道了两种 STK11 异构体,一种具有 C 末端变异的选择性剪接异构体,主要在睾丸中表达(LKB1)。另一种具有致癌特性的异构体在其 N 末端缺失几个残基(ΔN-LKB1)。在本研究中,我们报告了一种新的转录变体 Stk11N 的鉴定,该变体通过选择性剪接产生。在小鼠的出生后 7 天和成年阶段,发现新变体具有差异和组织特异性表达。与已知的变体 Stk11C 相比,新变体的概念性翻译氨基酸序列从外显子-E2 开始不同。新变体和已发表变体的计算机后翻译研究表明,某些特性相似,而在核输出信号、磷酸化、糖基化等特性上存在差异。因此,Stk11 基因的选择性剪接产生具有异质特性的新变体,表明这些变体在控制 AMPK 通路和其他功能方面存在复杂的调节。

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