Ariizumi Tohru, Hatakeyama Katsunori, Hinata Kokichi, Inatsugi Rie, Nishida Ikuo, Sato Shusei, Kato Tomohiko, Tabata Satoshi, Toriyama Kinya
Laboratory of Plant Breeding and Genetics, Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai 981-8555, Japan.
Plant J. 2004 Jul;39(2):170-81. doi: 10.1111/j.1365-313X.2004.02118.x.
A novel male-sterile mutant of Arabidopsis thaliana was isolated by means of T-DNA tagging. Pollen abortion of the mutant was evident after microspore release, and pollen grains were completely absent at anthesis. Transmission electron microscope analysis revealed that primexine was coarsely developed, and that although sporopollenin was produced, it was not deposited onto the microspore plasma membrane. The sporopollenin that failed to be deposited aggregated and accumulated within the locule and on the locule wall. Finally, as no exine formation was observed, the mutant was named nef1. The plastoglobuli within the plastids of the tapetum were reduced, and lipid accumulation was considerably decreased. The mutant had a significantly altered leaf chloroplast ultrastructure and showed various growth defects. Lipid analysis revealed that the total lipid content in nef1 was lower than that in the wild type, which indicated that Nef1 was involved in lipid metabolism. Cloning of the full-length Nef1 indicated that the gene encodes a novel plant protein of 1123 amino acids with limited sequence similarities to membrane proteins or transporter-like proteins, and the NEF1 is predicted to be a plastid integral membrane protein. Motif analysis revealed that NEF1 contains prokaryotic membrane lipoprotein lipid attachment sites that are involved in maintaining cell envelope integrity. It is predicted that the Nef1 encodes a membrane protein that maintains the envelope integrity in the plastids.
通过T-DNA标签法分离出一种拟南芥新型雄性不育突变体。突变体的花粉在小孢子释放后明显败育,花期时完全没有花粉粒。透射电子显微镜分析显示,花粉外壁的外壁外层发育粗糙,尽管产生了孢粉素,但未沉积在小孢子质膜上。未能沉积的孢粉素在小孢子囊内和小孢子囊壁上聚集和积累。最后,由于未观察到外壁形成,该突变体被命名为nef1。绒毡层质体中的质体小球减少,脂质积累显著降低。该突变体叶片叶绿体超微结构发生显著改变,并表现出各种生长缺陷。脂质分析表明,nef1中的总脂质含量低于野生型,这表明Nef1参与脂质代谢。全长Nef1的克隆表明,该基因编码一种由1123个氨基酸组成的新型植物蛋白,与膜蛋白或转运蛋白样蛋白的序列相似性有限,并且NEF1预计是一种质体整合膜蛋白。基序分析表明,NEF1含有原核膜脂蛋白脂质附着位点,这些位点参与维持细胞膜完整性。预计Nef1编码一种维持质体包膜完整性的膜蛋白。