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甘薯野生祖先(H.B.K.)中NBS编码基因的全基因组鉴定与特征分析。

Genome-wide identification and characterization of NBS-encoding genes in the sweet potato wild ancestor (H.B.K.).

作者信息

Si Zengzhi, Qiao Yake, Zhang Kai, Ji Zhixin, Han Jinling

机构信息

Hebei Key Laboratory of Crop Stress Biology, Hebei Normal University of Science & Technology, Qinghuangdao, 066000, Hebei Province, China.

出版信息

Open Life Sci. 2022 May 12;17(1):497-511. doi: 10.1515/biol-2022-0052. eCollection 2022.

DOI:10.1515/biol-2022-0052
PMID:35647293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9102303/
Abstract

The most predominant type of resistance (R) genes contain nucleotide-binding sites and leucine-rich repeat (NBS-LRR) domains, characterization of which is helpful for plant resistance improvement. However, the NBS genes of (H.B.K.) remain insufficient to date. In this study, a genome-wide analysis of the NBS-encoding gene in (H.B.K.) was carried out. A total of 442 NBS encoding genes were identified, amounting to 1.37% of the total genes of (H.B.K.). Based on the analysis of the domains, the identified genes were further classified into seven groups: CNL, NL, CN, N, TNL, TN, and RNL. Phylogenetic analysis showed that the NBS genes clustered into three independent clades: RNL, TNL, and CNL. Chromosome location analysis revealed that the distribution of genes in chromosomes was uneven, with a number ranging from 3 to 45. Multiple stress-related regulatory elements were detected in the promoters of the NBS-encoding genes, and their expression profiles were obtained. The qRT-PCR analysis revealed that , , , and 88 responded to stem nematode infection. These results provide critical proof for further characterization and analysis of NBS-encoding genes with important functions.

摘要

最主要的抗性(R)基因类型包含核苷酸结合位点和富含亮氨酸重复序列(NBS-LRR)结构域,对其进行表征有助于提高植物抗性。然而,迄今为止,(H.B.K.)的NBS基因仍然不足。在本研究中,对(H.B.K.)中编码NBS的基因进行了全基因组分析。共鉴定出442个编码NBS的基因,占(H.B.K.)总基因数的1.37%。基于结构域分析,将鉴定出的基因进一步分为七组:CNL、NL、CN、N、TNL、TN和RNL。系统发育分析表明,(H.B.K.)的NBS基因聚为三个独立的进化枝:RNL、TNL和CNL。染色体定位分析显示,(H.B.K.)基因在染色体上的分布不均匀,数量从3到45不等。在编码NBS的基因启动子中检测到多个与胁迫相关的调控元件,并获得了它们的表达谱。qRT-PCR分析表明,(基因名称未给出)、(基因名称未给出)、(基因名称未给出)和88个基因对茎线虫感染有响应。这些结果为进一步表征和分析具有重要功能的编码NBS的基因提供了关键证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/ee5d7e420abc/j_biol-2022-0052-fig007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/1f7b695b3294/j_biol-2022-0052-fig001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/bcc0734da454/j_biol-2022-0052-fig002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/ced8299df38a/j_biol-2022-0052-fig003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/f8ec7de3e08e/j_biol-2022-0052-fig004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/fda909c3342b/j_biol-2022-0052-fig005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/d122c023545b/j_biol-2022-0052-fig006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/ee5d7e420abc/j_biol-2022-0052-fig007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/1f7b695b3294/j_biol-2022-0052-fig001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/bcc0734da454/j_biol-2022-0052-fig002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/ced8299df38a/j_biol-2022-0052-fig003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/f8ec7de3e08e/j_biol-2022-0052-fig004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/fda909c3342b/j_biol-2022-0052-fig005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/d122c023545b/j_biol-2022-0052-fig006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12a3/9102303/ee5d7e420abc/j_biol-2022-0052-fig007.jpg

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