Identification of a Gravitropism-Deficient Mutant in Rice

A gravitropism-deficient mutant M96 was isolated from a mutant bank, generated by ethyl methane sulfonate (EMS) mutagenesis of indica rice accession ZJ100. The mutant was characterized as prostrate growth at the beginning of germination, and the prostrate growth phenotype ran through the whole life...

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Main Authors: He Yan, Shi Yong-feng, Zhang Xiao-bo, Wang Hui-mei, Xu Xia, Wu Jian-li
Format: Article
Language:English
Published: Elsevier 2017-03-01
Series:Rice Science
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1672630817300057
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spelling doaj-219f0c0b81824f0cb24ad718739921f62020-11-24T23:55:32ZengElsevierRice Science1672-63082017-03-0124210911810.1016/j.rsci.2016.06.009Identification of a Gravitropism-Deficient Mutant in RiceHe YanShi Yong-fengZhang Xiao-boWang Hui-meiXu XiaWu Jian-liA gravitropism-deficient mutant M96 was isolated from a mutant bank, generated by ethyl methane sulfonate (EMS) mutagenesis of indica rice accession ZJ100. The mutant was characterized as prostrate growth at the beginning of germination, and the prostrate growth phenotype ran through the whole life duration. Tiller angle and tiller number of M96 increased significantly in comparison with the wild type. Tissue section observation analysis indicated that asymmetric stem growth around the second node occurred in M96. Genetic analysis and gene mapping showed that M96 was controlled by a single recessive nuclear gene, tentatively termed as gravitropism-deficient M96 (gdM96), which was mapped to a region of 506 kb flanked by markers RM5960 and InDel8 on the long arm of chromosome 11. Sequencing analysis of the open reading frames in this region revealed a nucleotide substitution from G to T in the third exon of LOC_Os11g29840. Additionally, real-time fluorescence quantitative PCR analysis showed that the expression level of LOC_Os11g29840 in the stems was much higher than in the roots and leaves in M96. Furthermore, the expression level was more than four times in M96 stem than in the wild type stem. Our results suggested that the mutant gene was likely a new allele to the reported gene LAZY1. Isolation of this new allele would facilitate the further characterization of LAZY1.http://www.sciencedirect.com/science/article/pii/S1672630817300057plant architecturegravitropismLAZY1gene mappingmutant
collection DOAJ
language English
format Article
sources DOAJ
author He Yan
Shi Yong-feng
Zhang Xiao-bo
Wang Hui-mei
Xu Xia
Wu Jian-li
spellingShingle He Yan
Shi Yong-feng
Zhang Xiao-bo
Wang Hui-mei
Xu Xia
Wu Jian-li
Identification of a Gravitropism-Deficient Mutant in Rice
Rice Science
plant architecture
gravitropism
LAZY1
gene mapping
mutant
author_facet He Yan
Shi Yong-feng
Zhang Xiao-bo
Wang Hui-mei
Xu Xia
Wu Jian-li
author_sort He Yan
title Identification of a Gravitropism-Deficient Mutant in Rice
title_short Identification of a Gravitropism-Deficient Mutant in Rice
title_full Identification of a Gravitropism-Deficient Mutant in Rice
title_fullStr Identification of a Gravitropism-Deficient Mutant in Rice
title_full_unstemmed Identification of a Gravitropism-Deficient Mutant in Rice
title_sort identification of a gravitropism-deficient mutant in rice
publisher Elsevier
series Rice Science
issn 1672-6308
publishDate 2017-03-01
description A gravitropism-deficient mutant M96 was isolated from a mutant bank, generated by ethyl methane sulfonate (EMS) mutagenesis of indica rice accession ZJ100. The mutant was characterized as prostrate growth at the beginning of germination, and the prostrate growth phenotype ran through the whole life duration. Tiller angle and tiller number of M96 increased significantly in comparison with the wild type. Tissue section observation analysis indicated that asymmetric stem growth around the second node occurred in M96. Genetic analysis and gene mapping showed that M96 was controlled by a single recessive nuclear gene, tentatively termed as gravitropism-deficient M96 (gdM96), which was mapped to a region of 506 kb flanked by markers RM5960 and InDel8 on the long arm of chromosome 11. Sequencing analysis of the open reading frames in this region revealed a nucleotide substitution from G to T in the third exon of LOC_Os11g29840. Additionally, real-time fluorescence quantitative PCR analysis showed that the expression level of LOC_Os11g29840 in the stems was much higher than in the roots and leaves in M96. Furthermore, the expression level was more than four times in M96 stem than in the wild type stem. Our results suggested that the mutant gene was likely a new allele to the reported gene LAZY1. Isolation of this new allele would facilitate the further characterization of LAZY1.
topic plant architecture
gravitropism
LAZY1
gene mapping
mutant
url http://www.sciencedirect.com/science/article/pii/S1672630817300057
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