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Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum
BACKGROUND: Virescent mutation broadly exists in plants and is an ideal experimental material to investigate regulatory mechanisms underlying chlorophyll synthesis, photosynthesis and plant growth. Up to date, the molecular mechanisms in two virescent mutations have been clarified in cottons (Gossyp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254239/ https://www.ncbi.nlm.nih.gov/pubmed/34217203 http://dx.doi.org/10.1186/s12864-021-07810-z |
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author | Gao, Jin Shi, Yang Wang, Wei Wang, Yong-Hui Yang, Hua Shi, Qing-Hua Chen, Jian-Ping Sun, Yan-Ru Cai, Li-Wang |
author_facet | Gao, Jin Shi, Yang Wang, Wei Wang, Yong-Hui Yang, Hua Shi, Qing-Hua Chen, Jian-Ping Sun, Yan-Ru Cai, Li-Wang |
author_sort | Gao, Jin |
collection | PubMed |
description | BACKGROUND: Virescent mutation broadly exists in plants and is an ideal experimental material to investigate regulatory mechanisms underlying chlorophyll synthesis, photosynthesis and plant growth. Up to date, the molecular mechanisms in two virescent mutations have been clarified in cottons (Gossypiuma hirsutum). A virescent mutation has been found in the cotton strain Sumian 22, and the underlying molecular mechanisms have been studied. METHODS: The virescent mutant and wild type (WT) of Sumian 22 were cross-bred, and the F(1) population were self-pollinated to calculate the segregation ratio. Green and yellow leaves from F(2) populations were subjected to genome sequencing and bulked-segregant analysis was performed to screen mutations. Real-time quantitative PCR (RT-qPCR) were performed to identify genes in relations to chlorophyll synthesis. Intermediate products for chlorophyll synthesis were determined to validate the RT-qPCR results. RESULTS: The segregation ratio of green and virescent plants in F2 population complied with 3:1. Compared with WT, a 0.34 Mb highly mutated interval was identified on the chromosome D10 in mutant, which contained 31 genes. Among them, only ABCI1 displayed significantly lower levels in mutant than in WT. Meanwhile, the contents of Mg-protoporphyrin IX, protochlorophyllide, chlorophyll a and b were all significantly lower in mutant than in WT, which were consistent with the inhibited levels of ABCI1. In addition, a mutation from A to T at the -317 bp position from the start codon of ABCI1 was observed in the genome sequence of mutant. CONCLUSIONS: Inhibited transcription of ABCI1 might be the mechanism causing virescent mutation in Sumian 22 cotton, which reduced the transportation of protoporphyrin IX to plastid, and then inhibited Mg-protoporphyrin IX, Protochlorophyllide and finally chlorophyll synthesis. These results provided novel insights into the molecular mechanisms underlying virescent mutation in cotton. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07810-z. |
format | Online Article Text |
id | pubmed-8254239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82542392021-07-06 Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum Gao, Jin Shi, Yang Wang, Wei Wang, Yong-Hui Yang, Hua Shi, Qing-Hua Chen, Jian-Ping Sun, Yan-Ru Cai, Li-Wang BMC Genomics Research BACKGROUND: Virescent mutation broadly exists in plants and is an ideal experimental material to investigate regulatory mechanisms underlying chlorophyll synthesis, photosynthesis and plant growth. Up to date, the molecular mechanisms in two virescent mutations have been clarified in cottons (Gossypiuma hirsutum). A virescent mutation has been found in the cotton strain Sumian 22, and the underlying molecular mechanisms have been studied. METHODS: The virescent mutant and wild type (WT) of Sumian 22 were cross-bred, and the F(1) population were self-pollinated to calculate the segregation ratio. Green and yellow leaves from F(2) populations were subjected to genome sequencing and bulked-segregant analysis was performed to screen mutations. Real-time quantitative PCR (RT-qPCR) were performed to identify genes in relations to chlorophyll synthesis. Intermediate products for chlorophyll synthesis were determined to validate the RT-qPCR results. RESULTS: The segregation ratio of green and virescent plants in F2 population complied with 3:1. Compared with WT, a 0.34 Mb highly mutated interval was identified on the chromosome D10 in mutant, which contained 31 genes. Among them, only ABCI1 displayed significantly lower levels in mutant than in WT. Meanwhile, the contents of Mg-protoporphyrin IX, protochlorophyllide, chlorophyll a and b were all significantly lower in mutant than in WT, which were consistent with the inhibited levels of ABCI1. In addition, a mutation from A to T at the -317 bp position from the start codon of ABCI1 was observed in the genome sequence of mutant. CONCLUSIONS: Inhibited transcription of ABCI1 might be the mechanism causing virescent mutation in Sumian 22 cotton, which reduced the transportation of protoporphyrin IX to plastid, and then inhibited Mg-protoporphyrin IX, Protochlorophyllide and finally chlorophyll synthesis. These results provided novel insights into the molecular mechanisms underlying virescent mutation in cotton. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07810-z. BioMed Central 2021-07-03 /pmc/articles/PMC8254239/ /pubmed/34217203 http://dx.doi.org/10.1186/s12864-021-07810-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Gao, Jin Shi, Yang Wang, Wei Wang, Yong-Hui Yang, Hua Shi, Qing-Hua Chen, Jian-Ping Sun, Yan-Ru Cai, Li-Wang Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum |
title | Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum |
title_full | Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum |
title_fullStr | Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum |
title_full_unstemmed | Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum |
title_short | Genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton Gossypiuma hirsutum |
title_sort | genome sequencing identified novel mechanisms underlying virescent mutation in upland cotton gossypiuma hirsutum |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254239/ https://www.ncbi.nlm.nih.gov/pubmed/34217203 http://dx.doi.org/10.1186/s12864-021-07810-z |
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