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Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut

Plants usually respond to the external environment by initiating a series of signal transduction processes mediated by protein kinases, especially calcineurin B-like protein–interacting protein kinases (CIPKs). In this study, 54 CIPKs were identified in the peanut genome, of which 26 were from culti...

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Autores principales: Ren, Weifang, Zhang, Juncheng, He, Jie, Fang, Jiahai, Wan, Liyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483126/
https://www.ncbi.nlm.nih.gov/pubmed/36134030
http://dx.doi.org/10.3389/fgene.2022.939255
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author Ren, Weifang
Zhang, Juncheng
He, Jie
Fang, Jiahai
Wan, Liyun
author_facet Ren, Weifang
Zhang, Juncheng
He, Jie
Fang, Jiahai
Wan, Liyun
author_sort Ren, Weifang
collection PubMed
description Plants usually respond to the external environment by initiating a series of signal transduction processes mediated by protein kinases, especially calcineurin B-like protein–interacting protein kinases (CIPKs). In this study, 54 CIPKs were identified in the peanut genome, of which 26 were from cultivated species (named AhCIPKs) and 28 from two diploid progenitors (Arachis duranensis—AdCIPKs and Arachis ipaensis—AiCIPKs). Evolution analysis revealed that the 54 CIPKs were composed of two different evolutionary branches. The CIPK members were unevenly distributed at different chromosomes. Synteny analysis strongly indicated that whole-genome duplication (allopolyploidization) contributed to the expansion of CIPK. Comparative genomics analysis showed that there was only one common collinear CIPK pairs among peanut, Arabidopsis, rice, grape, and soybean. The prediction results of cis-acting elements showed that AhCIPKs, AdCIPKs, and AiCIPKs contained different proportions of transcription factor binding motifs involved in regulating plant growth, abiotic stress, plant hormones, and light response elements. Spatial expression profiles revealed that almost all AhCIPKs had tissue-specific expression patterns. Furthermore, association analysis identified one polymorphic site in AdCIPK12 (AhCIPK11), which was significantly associated with pod length, seed length, hundred seed weight, and shoot root ratio. Our results provide valuable information of CIPKs in peanut and facilitate better understanding of their biological functions.
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spelling pubmed-94831262022-09-20 Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut Ren, Weifang Zhang, Juncheng He, Jie Fang, Jiahai Wan, Liyun Front Genet Genetics Plants usually respond to the external environment by initiating a series of signal transduction processes mediated by protein kinases, especially calcineurin B-like protein–interacting protein kinases (CIPKs). In this study, 54 CIPKs were identified in the peanut genome, of which 26 were from cultivated species (named AhCIPKs) and 28 from two diploid progenitors (Arachis duranensis—AdCIPKs and Arachis ipaensis—AiCIPKs). Evolution analysis revealed that the 54 CIPKs were composed of two different evolutionary branches. The CIPK members were unevenly distributed at different chromosomes. Synteny analysis strongly indicated that whole-genome duplication (allopolyploidization) contributed to the expansion of CIPK. Comparative genomics analysis showed that there was only one common collinear CIPK pairs among peanut, Arabidopsis, rice, grape, and soybean. The prediction results of cis-acting elements showed that AhCIPKs, AdCIPKs, and AiCIPKs contained different proportions of transcription factor binding motifs involved in regulating plant growth, abiotic stress, plant hormones, and light response elements. Spatial expression profiles revealed that almost all AhCIPKs had tissue-specific expression patterns. Furthermore, association analysis identified one polymorphic site in AdCIPK12 (AhCIPK11), which was significantly associated with pod length, seed length, hundred seed weight, and shoot root ratio. Our results provide valuable information of CIPKs in peanut and facilitate better understanding of their biological functions. Frontiers Media S.A. 2022-09-05 /pmc/articles/PMC9483126/ /pubmed/36134030 http://dx.doi.org/10.3389/fgene.2022.939255 Text en Copyright © 2022 Ren, Zhang, He, Fang and Wan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Ren, Weifang
Zhang, Juncheng
He, Jie
Fang, Jiahai
Wan, Liyun
Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut
title Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut
title_full Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut
title_fullStr Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut
title_full_unstemmed Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut
title_short Identification, expression, and association analysis of calcineurin B-like protein–interacting protein kinase genes in peanut
title_sort identification, expression, and association analysis of calcineurin b-like protein–interacting protein kinase genes in peanut
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483126/
https://www.ncbi.nlm.nih.gov/pubmed/36134030
http://dx.doi.org/10.3389/fgene.2022.939255
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