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水稻中WNK激酶基因家族的全基因组鉴定与表达分析

Genome-wide identification and expression analysis of WNK kinase gene family in rice.

作者信息

Manuka Rakesh, Saddhe Ankush Ashok, Kumar Kundan

机构信息

Department of Biological Sciences, Birla Institute of Technology & Science Pilani, K.K. Birla Goa Campus, Goa 403726, India.

Department of Biological Sciences, Birla Institute of Technology & Science Pilani, K.K. Birla Goa Campus, Goa 403726, India.

出版信息

Comput Biol Chem. 2015 Dec;59 Pt A:56-66. doi: 10.1016/j.compbiolchem.2015.09.003. Epub 2015 Sep 8.

Abstract

Eukaryotic protein kinases represent one of the largest gene families involved in diverse regulatory functions. WNK (With No Lysine) kinases are members of ser/thr protein kinase family, which lack conserved catalytic lysine (K) residue at protein kinase subdomain II and is replaced by either asparagine, serine or glycine residues. They are involved in regulation of flowering time, circadian rhythms and abiotic stresses in Arabidopsis thaliana. In the present study, we have identified 9 members of WNK in rice, showed resemblance to Arabidopsis and human WNK and clustered into five main clades phylogenetically. The predicted genes structure, bonafide conserved signature motif and domains strongly support their identity, as members of WNK kinase family. We have analyzed their chromosomal distribution, physio-chemical properties, subcellular localizations and cis-elements in the promoter regions in silico. Further, transcript analysis of OsWNK by qRT-PCR revealed their differential regulation in tissue specific and abiotic stresses libraries. In conclusion, the identification of nine OsWNK and transcript level expression pattern under abiotic stress using qRT-PCR in rice will significantly contribute towards the understanding of WNK genes in monocots and thus provide a set up for functional genomics studies of WNK protein kinases.

摘要

真核蛋白激酶是参与多种调控功能的最大基因家族之一。WNK(无赖氨酸)激酶是丝氨酸/苏氨酸蛋白激酶家族的成员,在蛋白激酶亚结构域II中缺乏保守的催化赖氨酸(K)残基,取而代之的是天冬酰胺、丝氨酸或甘氨酸残基。它们参与拟南芥开花时间、昼夜节律和非生物胁迫的调控。在本研究中,我们在水稻中鉴定出9个WNK成员,它们与拟南芥和人类的WNK相似,并在系统发育上聚为五个主要分支。预测的基因结构、真正保守的特征基序和结构域有力地支持了它们作为WNK激酶家族成员的身份。我们在计算机上分析了它们的染色体分布、理化性质、亚细胞定位和启动子区域的顺式元件。此外,通过qRT-PCR对OsWNK进行转录分析,揭示了它们在组织特异性和非生物胁迫文库中的差异调控。总之,在水稻中鉴定出9个OsWNK并利用qRT-PCR分析其在非生物胁迫下的转录水平表达模式,将极大地有助于理解单子叶植物中的WNK基因,从而为WNK蛋白激酶的功能基因组学研究提供一个平台。

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