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水稻(Oryza sativa L. japonica)基因组中 GDSL 酯酶/脂肪酶基因家族的多功能性和多样性:生物信息学分析的新见解。

Multifunctionality and diversity of GDSL esterase/lipase gene family in rice (Oryza sativa L. japonica) genome: new insights from bioinformatics analysis.

机构信息

Department of Food Science and Biotechnology, National Chung Hsing University, Taichung, Taiwan 402, ROC.

出版信息

BMC Genomics. 2012 Jul 15;13:309. doi: 10.1186/1471-2164-13-309.

DOI:10.1186/1471-2164-13-309
PMID:22793791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3412167/
Abstract

BACKGROUND

GDSL esterases/lipases are a newly discovered subclass of lipolytic enzymes that are very important and attractive research subjects because of their multifunctional properties, such as broad substrate specificity and regiospecificity. Compared with the current knowledge regarding these enzymes in bacteria, our understanding of the plant GDSL enzymes is very limited, although the GDSL gene family in plant species include numerous members in many fully sequenced plant genomes. Only two genes from a large rice GDSL esterase/lipase gene family were previously characterised, and the majority of the members remain unknown. In the present study, we describe the rice OsGELP (Oryza sativa GDSL esterase/lipase protein) gene family at the genomic and proteomic levels, and use this knowledge to provide insights into the multifunctionality of the rice OsGELP enzymes.

RESULTS

In this study, an extensive bioinformatics analysis identified 114 genes in the rice OsGELP gene family. A complete overview of this family in rice is presented, including the chromosome locations, gene structures, phylogeny, and protein motifs. Among the OsGELPs and the plant GDSL esterase/lipase proteins of known functions, 41 motifs were found that represent the core secondary structure elements or appear specifically in different phylogenetic subclades. The specification and distribution of identified putative conserved clade-common and -specific peptide motifs, and their location on the predicted protein three dimensional structure may possibly signify their functional roles. Potentially important regions for substrate specificity are highlighted, in accordance with protein three-dimensional model and location of the phylogenetic specific conserved motifs. The differential expression of some representative genes were confirmed by quantitative real-time PCR. The phylogenetic analysis, together with protein motif architectures, and the expression profiling were analysed to predict the possible biological functions of the rice OsGELP genes.

CONCLUSIONS

Our current genomic analysis, for the first time, presents fundamental information on the organization of the rice OsGELP gene family. With combination of the genomic, phylogenetic, microarray expression, protein motif distribution, and protein structure analyses, we were able to create supported basis for the functional prediction of many members in the rice GDSL esterase/lipase family. The present study provides a platform for the selection of candidate genes for further detailed functional study.

摘要

背景

GDSL 酯酶/脂肪酶是一类新发现的脂肪酶,由于其多功能特性,如广泛的底物特异性和区域特异性,因此是非常重要和有吸引力的研究对象。与目前关于细菌中这些酶的知识相比,尽管植物物种中的 GDSL 基因家族在许多完全测序的植物基因组中包含许多成员,但我们对植物 GDSL 酶的了解非常有限。以前仅对来自大型水稻 GDSL 酯酶/脂肪酶基因家族的两个基因进行了表征,而大多数成员仍未知。在本研究中,我们在基因组和蛋白质组水平上描述了水稻 OsGELP(Oryza sativa GDSL 酯酶/脂肪酶蛋白)基因家族,并利用这些知识深入了解水稻 OsGELP 酶的多功能性。

结果

在这项研究中,通过广泛的生物信息学分析,在水稻 OsGELP 基因家族中鉴定出 114 个基因。本文全面介绍了该家族在水稻中的情况,包括染色体位置、基因结构、系统发育和蛋白质基序。在 OsGELPs 和已知功能的植物 GDSL 酯酶/脂肪酶蛋白中,发现了 41 个基序,这些基序代表了核心二级结构元素或专门出现在不同的系统发育亚群中。鉴定出的假定保守簇共同和特异性肽基序的特异性和分布及其在预测蛋白质三维结构上的位置,可能表明其功能作用。根据蛋白质三维模型和系统发育特异性保守基序的位置,突出了可能对底物特异性很重要的区域。通过定量实时 PCR 验证了一些代表性基因的差异表达。通过系统发育分析、蛋白质基序结构以及表达谱分析,预测了水稻 OsGELP 基因的可能生物学功能。

结论

我们目前的基因组分析首次提供了有关水稻 OsGELP 基因家族组织的基本信息。通过基因组、系统发育、微阵列表达、蛋白质基序分布和蛋白质结构分析的组合,我们能够为水稻 GDSL 酯酶/脂肪酶家族中许多成员的功能预测提供支持基础。本研究为进一步详细功能研究的候选基因选择提供了平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/079f5ad6da39/1471-2164-13-309-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/e296b1211705/1471-2164-13-309-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/256aa55c628a/1471-2164-13-309-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/ce83fc994089/1471-2164-13-309-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/1ed2610d0a21/1471-2164-13-309-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/60664b1cc045/1471-2164-13-309-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/079f5ad6da39/1471-2164-13-309-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/e296b1211705/1471-2164-13-309-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/256aa55c628a/1471-2164-13-309-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/ce83fc994089/1471-2164-13-309-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/1ed2610d0a21/1471-2164-13-309-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/60664b1cc045/1471-2164-13-309-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/3412167/079f5ad6da39/1471-2164-13-309-6.jpg

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