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MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum)

MSH2 is the core protein of MutS‐homolog family involved in recognition and repair of the errors in the DNA. While other members of MutS‐homolog family reportedly regulate mitochondrial stability, meiosis, and fertility, MSH2 is believed to participate mainly in mismatch repair. The search for polym...

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Autores principales: Sarma, Supriya, Pandey, Arun Kumar, Sharma, Kapil, Ravi, Maruthachalam, Sreelakshmi, Yellamaraju, Sharma, Rameshwar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508528/
https://www.ncbi.nlm.nih.gov/pubmed/31245679
http://dx.doi.org/10.1002/pld3.17
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author Sarma, Supriya
Pandey, Arun Kumar
Sharma, Kapil
Ravi, Maruthachalam
Sreelakshmi, Yellamaraju
Sharma, Rameshwar
author_facet Sarma, Supriya
Pandey, Arun Kumar
Sharma, Kapil
Ravi, Maruthachalam
Sreelakshmi, Yellamaraju
Sharma, Rameshwar
author_sort Sarma, Supriya
collection PubMed
description MSH2 is the core protein of MutS‐homolog family involved in recognition and repair of the errors in the DNA. While other members of MutS‐homolog family reportedly regulate mitochondrial stability, meiosis, and fertility, MSH2 is believed to participate mainly in mismatch repair. The search for polymorphism in MSH2 sequence in tomato accessions revealed both synonymous and nonsynonymous SNPs; however, SIFT algorithm predicted that none of the SNPs influenced MSH2 protein function. The silencing of MSH2 gene expression by RNAi led to phenotypic abnormalities in highly silenced lines, particularly in the stamens with highly reduced pollen formation. MSH2 silencing exacerbated formation of UV‐B‐induced thymine dimers and blocked light‐induced repair of the dimers. The MSH2 silencing also affected the progression of male meiosis to a varying degree with either halt of meiosis at zygotene stage or formation of diploid tetrads. The immunostaining of male meiocytes with centromere localized CENPC (centromere protein C) antibody showed the presence of 48 univalent along with 24 bivalent chromosomes suggesting abnormal tetraploid meiosis. The mitotic cells of root tips of silenced lines showed diploid nuclei but lacked intervening cell plates leading to cells with syncytial nuclei. Thus, we speculate that tetraploid pollen mother cells may have arisen due to the fusion of syncytial nuclei before the onset of meiosis. It is likely that in addition to mismatch repair (MMR), MSH2 may have an additional role in regulating ploidy stability.
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spelling pubmed-65085282019-06-26 MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum) Sarma, Supriya Pandey, Arun Kumar Sharma, Kapil Ravi, Maruthachalam Sreelakshmi, Yellamaraju Sharma, Rameshwar Plant Direct Original Research MSH2 is the core protein of MutS‐homolog family involved in recognition and repair of the errors in the DNA. While other members of MutS‐homolog family reportedly regulate mitochondrial stability, meiosis, and fertility, MSH2 is believed to participate mainly in mismatch repair. The search for polymorphism in MSH2 sequence in tomato accessions revealed both synonymous and nonsynonymous SNPs; however, SIFT algorithm predicted that none of the SNPs influenced MSH2 protein function. The silencing of MSH2 gene expression by RNAi led to phenotypic abnormalities in highly silenced lines, particularly in the stamens with highly reduced pollen formation. MSH2 silencing exacerbated formation of UV‐B‐induced thymine dimers and blocked light‐induced repair of the dimers. The MSH2 silencing also affected the progression of male meiosis to a varying degree with either halt of meiosis at zygotene stage or formation of diploid tetrads. The immunostaining of male meiocytes with centromere localized CENPC (centromere protein C) antibody showed the presence of 48 univalent along with 24 bivalent chromosomes suggesting abnormal tetraploid meiosis. The mitotic cells of root tips of silenced lines showed diploid nuclei but lacked intervening cell plates leading to cells with syncytial nuclei. Thus, we speculate that tetraploid pollen mother cells may have arisen due to the fusion of syncytial nuclei before the onset of meiosis. It is likely that in addition to mismatch repair (MMR), MSH2 may have an additional role in regulating ploidy stability. John Wiley and Sons Inc. 2018-01-02 /pmc/articles/PMC6508528/ /pubmed/31245679 http://dx.doi.org/10.1002/pld3.17 Text en © 2018 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Sarma, Supriya
Pandey, Arun Kumar
Sharma, Kapil
Ravi, Maruthachalam
Sreelakshmi, Yellamaraju
Sharma, Rameshwar
MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum)
title MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum)
title_full MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum)
title_fullStr MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum)
title_full_unstemmed MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum)
title_short MutS‐Homolog2 silencing generates tetraploid meiocytes in tomato (Solanum lycopersicum)
title_sort muts‐homolog2 silencing generates tetraploid meiocytes in tomato (solanum lycopersicum)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508528/
https://www.ncbi.nlm.nih.gov/pubmed/31245679
http://dx.doi.org/10.1002/pld3.17
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