Hurtado Lidia, Farrona Sara, Reyes Jose C
Instituto de Bioquímica Vegetal y Fotosíntesis, Consejo Superior de Investigaciones Científicas-Universidad de Sevilla, Av. Américo Vespucio 49, E-41092 Sevilla, Spain.
Plant Mol Biol. 2006 Sep;62(1-2):291-304. doi: 10.1007/s11103-006-9021-2. Epub 2006 Jul 15.
Arabidopsis thaliana BRAHMA (BRM, also called AtBRM) is a SNF2 family protein homolog of Brahma, the ATPase of the Drosophila SWI/SNF complex involved in chromatin remodeling during transcription. Here we show that, in contrast to its Drosophila counterpart, BRM is not an essential gene. Thus, homozygous BRM loss of function mutants are viable but exhibit numerous defects including dwarfism, altered leaf and root development and several reproduction defects. The analysis of the progeny of self-fertilized heterozygous brm plants and reciprocal crosses between heterozygous and wild type plants indicated that disruption of BRM reduced both male and female gametophyte transmission. This was consistent with the presence of aborted ovules in the self-fertilized heterozygous flowers that contained arrested embryos predominantly at the two terminal cells stage. Furthermore, brm homozygous mutants were completely sterile. Flowers of brm loss-of-function mutants have several developmental abnormalities, including homeotic transformations in the second and third floral whorls. In accordance with these results, brm mutants present reduced levels of APETALA2, APETALA3, PISTILLATA and NAC-LIKE, ACTIVATED BY AP3/PI. We have previously shown that BRM strongly interacts with AtSWI3C. Now we extend our interaction studies demonstrating that BRM interacts weakly with AtSWI3B but not with AtSWI3A or AtSWI3D. In agreement with these results, the phenotype described in this study for brm plants is very similar to that previously described for the AtSWI3C mutant plants, suggesting that both proteins participate in the same genetic pathway or form a molecular complex.
拟南芥BRHAMA(BRM,也称为AtBRM)是果蝇Brahma的SNF2家族蛋白同源物,果蝇Brahma是果蝇SWI/SNF复合物中的ATP酶,参与转录过程中的染色质重塑。在此我们表明,与其果蝇对应物不同,BRM不是必需基因。因此,纯合的BRM功能缺失突变体是可存活的,但表现出许多缺陷,包括侏儒症、叶片和根系发育改变以及一些生殖缺陷。对自交杂合brm植株的后代以及杂合与野生型植株之间的正反交分析表明,BRM的破坏降低了雄配子体和雌配子体的传递。这与自交杂合花中存在败育胚珠一致,这些胚珠中的胚胎主要在两个末端细胞阶段停滞发育。此外,brm纯合突变体完全不育。brm功能缺失突变体的花有几个发育异常,包括第二轮和第三轮花器官的同源异型转变。与这些结果一致,brm突变体中APETALA2、APETALA3、PISTILLATA和由AP3/PI激活的NAC-LIKE水平降低。我们之前已经表明BRM与AtSWI3C强烈相互作用。现在我们扩展了相互作用研究,证明BRM与AtSWI3B弱相互作用,但与AtSWI3A或AtSWI3D不相互作用。与这些结果一致,本研究中描述的brm植株的表型与之前描述的AtSWI3C突变体植株的表型非常相似,这表明这两种蛋白参与相同的遗传途径或形成分子复合物。