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OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth
Aspartic proteases (APs) comprise a large proteolytic enzyme family widely distributed in animals, microbes, viruses, and plants. The rice genome encodes 96 APs, of which only a few have been functionally characterized. Here, the identification and characterization of a novel AP gene, OsAP65, which...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733154/ https://www.ncbi.nlm.nih.gov/pubmed/23918968 http://dx.doi.org/10.1093/jxb/ert173 |
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author | Huang, Jianyan Zhao, Xiaobo Cheng, Ke Jiang, Yunhe Ouyang, Yidan Xu, Caiguo Li, Xianghua Xiao, Jinghua Zhang, Qifa |
author_facet | Huang, Jianyan Zhao, Xiaobo Cheng, Ke Jiang, Yunhe Ouyang, Yidan Xu, Caiguo Li, Xianghua Xiao, Jinghua Zhang, Qifa |
author_sort | Huang, Jianyan |
collection | PubMed |
description | Aspartic proteases (APs) comprise a large proteolytic enzyme family widely distributed in animals, microbes, viruses, and plants. The rice genome encodes 96 APs, of which only a few have been functionally characterized. Here, the identification and characterization of a novel AP gene, OsAP65, which plays an indispensable role in pollen tube growth in rice, is reported. The T-DNA insertion line of OsAP65 caused severe segregation distortion. In the progeny derived from an individual heterozygous for the T-DNA insertion, the wild type and T-DNA-carrying heterozygote segregated at a ratio close to 1:1, while homozygotes of disrupted OsAP65 (OsAP65–/–) were not recovered. Reciprocal crosses between heterozygotes and wild-type plants demonstrated that the mutant alleles could not be transmitted through the male gamete. Examination of the anthers from heterozygous plants revealed that the mutant pollen matured normally, but did not germinate or elongate. OsAP65 was expressed in various tissues and the transcript level in heterozygous plants was about half of the amount measured in the wild-type plants. The subcellular localization showed that OsAP65 is a pre-vacuolar compartment (PVC) protein. These results indicated that OsAP65 was essential for rice pollen germination and tube growth. |
format | Online Article Text |
id | pubmed-3733154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37331542013-08-05 OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth Huang, Jianyan Zhao, Xiaobo Cheng, Ke Jiang, Yunhe Ouyang, Yidan Xu, Caiguo Li, Xianghua Xiao, Jinghua Zhang, Qifa J Exp Bot Research Paper Aspartic proteases (APs) comprise a large proteolytic enzyme family widely distributed in animals, microbes, viruses, and plants. The rice genome encodes 96 APs, of which only a few have been functionally characterized. Here, the identification and characterization of a novel AP gene, OsAP65, which plays an indispensable role in pollen tube growth in rice, is reported. The T-DNA insertion line of OsAP65 caused severe segregation distortion. In the progeny derived from an individual heterozygous for the T-DNA insertion, the wild type and T-DNA-carrying heterozygote segregated at a ratio close to 1:1, while homozygotes of disrupted OsAP65 (OsAP65–/–) were not recovered. Reciprocal crosses between heterozygotes and wild-type plants demonstrated that the mutant alleles could not be transmitted through the male gamete. Examination of the anthers from heterozygous plants revealed that the mutant pollen matured normally, but did not germinate or elongate. OsAP65 was expressed in various tissues and the transcript level in heterozygous plants was about half of the amount measured in the wild-type plants. The subcellular localization showed that OsAP65 is a pre-vacuolar compartment (PVC) protein. These results indicated that OsAP65 was essential for rice pollen germination and tube growth. Oxford University Press 2013-08 2013-07-30 /pmc/articles/PMC3733154/ /pubmed/23918968 http://dx.doi.org/10.1093/jxb/ert173 Text en © The Author [2013]. Published by Oxford University Press [on behalf of the Society for Experimental Biology]. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Paper Huang, Jianyan Zhao, Xiaobo Cheng, Ke Jiang, Yunhe Ouyang, Yidan Xu, Caiguo Li, Xianghua Xiao, Jinghua Zhang, Qifa OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth |
title | OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth |
title_full | OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth |
title_fullStr | OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth |
title_full_unstemmed | OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth |
title_short | OsAP65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth |
title_sort | osap65, a rice aspartic protease, is essential for male fertility and plays a role in pollen germination and pollen tube growth |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733154/ https://www.ncbi.nlm.nih.gov/pubmed/23918968 http://dx.doi.org/10.1093/jxb/ert173 |
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