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Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber
Leaf color mutants in higher plants are ideal materials for investigating the structure and function of photosynthetic system. In this study, we identified a cucumber vyl (virescent-yellow leaf) mutant in the mutant library, which exhibited reduced pigment contents and delayed chloroplast developmen...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897749/ https://www.ncbi.nlm.nih.gov/pubmed/29681911 http://dx.doi.org/10.3389/fpls.2018.00432 |
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author | Song, Mengfei Wei, Qingzhen Wang, Jing Fu, Wenyuan Qin, Xiaodong Lu, Xiumei Cheng, Feng Yang, Kang Zhang, Lu Yu, Xiaqing Li, Ji Chen, Jinfeng Lou, Qunfeng |
author_facet | Song, Mengfei Wei, Qingzhen Wang, Jing Fu, Wenyuan Qin, Xiaodong Lu, Xiumei Cheng, Feng Yang, Kang Zhang, Lu Yu, Xiaqing Li, Ji Chen, Jinfeng Lou, Qunfeng |
author_sort | Song, Mengfei |
collection | PubMed |
description | Leaf color mutants in higher plants are ideal materials for investigating the structure and function of photosynthetic system. In this study, we identified a cucumber vyl (virescent-yellow leaf) mutant in the mutant library, which exhibited reduced pigment contents and delayed chloroplast development process. F(2) and BC(1) populations were constructed from the cross between vyl mutant and cucumber inbred line ‘Hazerd’ to identify that the vyl trait is controlled by a simply recessive gene designated as CsVYL. The CsVYL gene was mapped to a 3.8 cM interval on chromosome 4 using these 80 F(2) individuals and BSA (bulked segregation analysis) approach. Fine genetic map was conducted with 1542 F(2) plants and narrowed down the vyl locus to an 86.3 kb genomic region, which contains a total of 11 genes. Sequence alignment between the wild type (WT) and vyl only identified one single nucleotide mutation (C→T) in the first exon of gene Csa4G637110, which encodes a DnaJ-like zinc finger protein. Gene Expression analysis confirmed the differences in transcription level of Csa4G637110 between wild type and mutant plants. Map-based cloning of the CsVYL gene could accelerate the study of chloroplast development and chlorophyll synthesis of cucumber. |
format | Online Article Text |
id | pubmed-5897749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58977492018-04-20 Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber Song, Mengfei Wei, Qingzhen Wang, Jing Fu, Wenyuan Qin, Xiaodong Lu, Xiumei Cheng, Feng Yang, Kang Zhang, Lu Yu, Xiaqing Li, Ji Chen, Jinfeng Lou, Qunfeng Front Plant Sci Plant Science Leaf color mutants in higher plants are ideal materials for investigating the structure and function of photosynthetic system. In this study, we identified a cucumber vyl (virescent-yellow leaf) mutant in the mutant library, which exhibited reduced pigment contents and delayed chloroplast development process. F(2) and BC(1) populations were constructed from the cross between vyl mutant and cucumber inbred line ‘Hazerd’ to identify that the vyl trait is controlled by a simply recessive gene designated as CsVYL. The CsVYL gene was mapped to a 3.8 cM interval on chromosome 4 using these 80 F(2) individuals and BSA (bulked segregation analysis) approach. Fine genetic map was conducted with 1542 F(2) plants and narrowed down the vyl locus to an 86.3 kb genomic region, which contains a total of 11 genes. Sequence alignment between the wild type (WT) and vyl only identified one single nucleotide mutation (C→T) in the first exon of gene Csa4G637110, which encodes a DnaJ-like zinc finger protein. Gene Expression analysis confirmed the differences in transcription level of Csa4G637110 between wild type and mutant plants. Map-based cloning of the CsVYL gene could accelerate the study of chloroplast development and chlorophyll synthesis of cucumber. Frontiers Media S.A. 2018-04-06 /pmc/articles/PMC5897749/ /pubmed/29681911 http://dx.doi.org/10.3389/fpls.2018.00432 Text en Copyright © 2018 Song, Wei, Wang, Fu, Qin, Lu, Cheng, Yang, Zhang, Yu, Li, Chen and Lou. http://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 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 | Plant Science Song, Mengfei Wei, Qingzhen Wang, Jing Fu, Wenyuan Qin, Xiaodong Lu, Xiumei Cheng, Feng Yang, Kang Zhang, Lu Yu, Xiaqing Li, Ji Chen, Jinfeng Lou, Qunfeng Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber |
title | Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber |
title_full | Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber |
title_fullStr | Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber |
title_full_unstemmed | Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber |
title_short | Fine Mapping of CsVYL, Conferring Virescent Leaf Through the Regulation of Chloroplast Development in Cucumber |
title_sort | fine mapping of csvyl, conferring virescent leaf through the regulation of chloroplast development in cucumber |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897749/ https://www.ncbi.nlm.nih.gov/pubmed/29681911 http://dx.doi.org/10.3389/fpls.2018.00432 |
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