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Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice

BACKGROUND: Intersubspecific autotetraploid rice hybrids possess high hybrid vigor; however, low pollen fertility is a critical hindrance in its commercial utilization. Our previous study demonstrated that polyploidy could increase the multi-loci interaction and cause high pollen abortion in autotet...

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Autores principales: Wu, Jinwen, Chen, Lin, Shahid, Muhammad Qasim, Chen, Minyi, Dong, Qinglei, Li, Jirui, Xu, Xiaosong, Liu, Xiangdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712294/
https://www.ncbi.nlm.nih.gov/pubmed/29197985
http://dx.doi.org/10.1186/s12284-017-0188-8
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author Wu, Jinwen
Chen, Lin
Shahid, Muhammad Qasim
Chen, Minyi
Dong, Qinglei
Li, Jirui
Xu, Xiaosong
Liu, Xiangdong
author_facet Wu, Jinwen
Chen, Lin
Shahid, Muhammad Qasim
Chen, Minyi
Dong, Qinglei
Li, Jirui
Xu, Xiaosong
Liu, Xiangdong
author_sort Wu, Jinwen
collection PubMed
description BACKGROUND: Intersubspecific autotetraploid rice hybrids possess high hybrid vigor; however, low pollen fertility is a critical hindrance in its commercial utilization. Our previous study demonstrated that polyploidy could increase the multi-loci interaction and cause high pollen abortion in autotetraploid rice hybrids. However, there is little known about the critical role of pollen sterility locus or loci in the intersubspecific hybrids. We developed autotetraploid rice hybrids harboring heterozygous genotypes (S (i) S (i) S (j) S (j)) at different pollen sterility loci by using the near isogenic lines of Taichung65-4×. Moreover, autotetraploid lines carrying double neutral genes, Sa (n) and Sb (n), were used to assess their effect on fertility restoration. RESULTS: Cytological studies showed that the deleterious genetic interactions at Sa and Sb pollen sterility loci resulted in higher pollen sterility (76.83%) and abnormal chromosome behavior (24.59%) at metaphase I of meiosis in autotetraploid rice hybrids. Transcriptome analysis revealed 1092 differentially expressed genes (DEG) in a hybrid with the pervasive interactions at Sa and Sb pollen sterility loci, and most of the genes (about 83%) exhibited down regulation. Of the DEG, 60 were associated with transcription regulation and 18 genes were annotated as meiosis-related genes. Analysis on the hybrids developed by using autotetraploid rice harboring double neutral genes, Sa (n) and Sb (n), revealed normal pollen fertility, and transcriptome analysis showed non-significant difference in number of DEG among different hybrids. CONCLUSIONS: Our finding revealed that pervasive interactions at Sa and Sb pollen sterility loci cause high sterility in the autotetraploid hybrids that lead to the down-regulation of important meiosis-related genes and transcription regulation factors. Moreover, we also found that the hybrids sterility could be overcome by double neutral genes, Sa (n) and Sb (n), in autotetraploid rice hybrids. The present study provided a strong evidence for the utilization of heterosis in autotetraploid rice hybrids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12284-017-0188-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-57122942017-12-07 Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice Wu, Jinwen Chen, Lin Shahid, Muhammad Qasim Chen, Minyi Dong, Qinglei Li, Jirui Xu, Xiaosong Liu, Xiangdong Rice (N Y) Original Article BACKGROUND: Intersubspecific autotetraploid rice hybrids possess high hybrid vigor; however, low pollen fertility is a critical hindrance in its commercial utilization. Our previous study demonstrated that polyploidy could increase the multi-loci interaction and cause high pollen abortion in autotetraploid rice hybrids. However, there is little known about the critical role of pollen sterility locus or loci in the intersubspecific hybrids. We developed autotetraploid rice hybrids harboring heterozygous genotypes (S (i) S (i) S (j) S (j)) at different pollen sterility loci by using the near isogenic lines of Taichung65-4×. Moreover, autotetraploid lines carrying double neutral genes, Sa (n) and Sb (n), were used to assess their effect on fertility restoration. RESULTS: Cytological studies showed that the deleterious genetic interactions at Sa and Sb pollen sterility loci resulted in higher pollen sterility (76.83%) and abnormal chromosome behavior (24.59%) at metaphase I of meiosis in autotetraploid rice hybrids. Transcriptome analysis revealed 1092 differentially expressed genes (DEG) in a hybrid with the pervasive interactions at Sa and Sb pollen sterility loci, and most of the genes (about 83%) exhibited down regulation. Of the DEG, 60 were associated with transcription regulation and 18 genes were annotated as meiosis-related genes. Analysis on the hybrids developed by using autotetraploid rice harboring double neutral genes, Sa (n) and Sb (n), revealed normal pollen fertility, and transcriptome analysis showed non-significant difference in number of DEG among different hybrids. CONCLUSIONS: Our finding revealed that pervasive interactions at Sa and Sb pollen sterility loci cause high sterility in the autotetraploid hybrids that lead to the down-regulation of important meiosis-related genes and transcription regulation factors. Moreover, we also found that the hybrids sterility could be overcome by double neutral genes, Sa (n) and Sb (n), in autotetraploid rice hybrids. The present study provided a strong evidence for the utilization of heterosis in autotetraploid rice hybrids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12284-017-0188-8) contains supplementary material, which is available to authorized users. Springer US 2017-12-02 /pmc/articles/PMC5712294/ /pubmed/29197985 http://dx.doi.org/10.1186/s12284-017-0188-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Wu, Jinwen
Chen, Lin
Shahid, Muhammad Qasim
Chen, Minyi
Dong, Qinglei
Li, Jirui
Xu, Xiaosong
Liu, Xiangdong
Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice
title Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice
title_full Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice
title_fullStr Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice
title_full_unstemmed Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice
title_short Pervasive interactions of Sa and Sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice
title_sort pervasive interactions of sa and sb loci cause high pollen sterility and abrupt changes in gene expression during meiosis that could be overcome by double neutral genes in autotetraploid rice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712294/
https://www.ncbi.nlm.nih.gov/pubmed/29197985
http://dx.doi.org/10.1186/s12284-017-0188-8
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