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水稻同源异型盒基因OSH15的功能缺失突变影响节间结构,导致植株矮化。

Loss-of-function mutations in the rice homeobox gene OSH15 affect the architecture of internodes resulting in dwarf plants.

作者信息

Sato Y, Sentoku N, Miura Y, Hirochika H, Kitano H, Matsuoka M

机构信息

Nagoya University, BioScience Center, Chikusa, Nagoya 464-8601, USA.

出版信息

EMBO J. 1999 Feb 15;18(4):992-1002. doi: 10.1093/emboj/18.4.992.

Abstract

The rice homeobox gene OSH15 (Oryza sativa homeobox) is a member of the knotted1-type homeobox gene family. We report here on the identification and characterization of a loss-of-function mutation in OSH15 from a library of retrotransposon-tagged lines of rice. Based on the phenotype and map position, we have identified three independent deletion alleles of the locus among conventional morphological mutants. All of these recessive mutations, which are considered to be null alleles, exhibit defects in internode elongation. Introduction of a 14 kbp genomic DNA fragment that includes all exons, introns and 5'- and 3'- flanking sequences of OSH15 complemented the defects in internode elongation, confirming that they were caused by the loss-of-function of OSH15. Internodes of the mutants had abnormal-shaped epidermal and hypodermal cells and showed an unusual arrangement of small vascular bundles. These mutations demonstrate a role for OSH15 in the development of rice internodes. This is the first evidence that the knotted1-type homeobox genes have roles other than shoot apical meristem formation and/or maintenance in plant development.

摘要

水稻同源异型框基因OSH15(Oryza sativa homeobox)是knotted1类同源异型框基因家族的成员。我们在此报告从水稻反转录转座子标签系文库中鉴定和表征OSH15功能缺失突变体的情况。基于表型和图谱位置,我们在常规形态突变体中鉴定出该位点的三个独立缺失等位基因。所有这些隐性突变被认为是无效等位基因,均表现出节间伸长缺陷。导入包含OSH15所有外显子、内含子以及5'和3'侧翼序列的14 kbp基因组DNA片段可弥补节间伸长缺陷,证实这些缺陷是由OSH15功能缺失所致。突变体的节间具有形状异常的表皮和皮下细胞,并且小维管束排列异常。这些突变证明了OSH15在水稻节间发育中的作用。这是knotted1类同源异型框基因在植物发育中除参与茎尖分生组织形成和/或维持之外还具有其他作用的首个证据。

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