DEX1是一种新的植物蛋白,在拟南芥花粉发育过程中参与了外叶模式的形成。

IF 6.5 1区 生物学 Q1 PLANT SCIENCES
Plant Physiology Pub Date : 2001-12-01 DOI:10.1104/PP.010517
D. M. Paxson-Sowders, C. Dodrill, Heather A. Owen, C. Makaroff
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引用次数: 199

摘要

为了确定正确花粉壁形成所需的因素,我们对拟南芥t - dna标记的dex1突变进行了表征,该突变导致花粉壁模式形成缺陷。本研究报道了DEX1的分离、分子鉴定以及DEX1植物的形态和超微结构分析。DEX1编码一种新的植物蛋白,该蛋白被预测与膜相关,并包含几个潜在的钙结合结构域。dex1植物的花粉壁发育与野生型植物相似,直到四分体早期。在dex1植物中,原胺沉积被延迟并显著减少。在野生型植物中观察到的正常质膜波纹和间隔物的产生在突变体中也不存在。在dex1植物中,孢粉素是产生并随机沉积在质膜上的。然而,它似乎并不固定在小孢子上,而是在发育中的小孢子和室壁上形成大的聚集体。根据DEX1的结构和DEX1植物的表型,提出了该蛋白的几种潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DEX1, a novel plant protein, is required for exine pattern formation during pollen development in Arabidopsis.
To identify factors that are required for proper pollen wall formation, we have characterized the T-DNA-tagged, dex1 mutation of Arabidopsis, which results in defective pollen wall pattern formation. This study reports the isolation and molecular characterization of DEX1 and morphological and ultrastructural analyses of dex1 plants. DEX1 encodes a novel plant protein that is predicted to be membrane associated and contains several potential calcium-binding domains. Pollen wall development in dex1 plants parallels that of wild-type plants until the early tetrad stage. In dex1 plants, primexine deposition is delayed and significantly reduced. The normal rippling of the plasma membrane and production of spacers observed in wild-type plants is also absent in the mutant. Sporopollenin is produced and randomly deposited on the plasma membrane in dex1 plants. However, it does not appear to be anchored to the microspore and forms large aggregates on the developing microspore and the locule walls. Based on the structure of DEX1 and the phenotype of dex1 plants, several potential roles for the protein are proposed.
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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
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