Reňák David, Dupl'áková Nikoleta, Honys David
Laboratory of Pollen Biology, Institute of Experimental Botany ASCR, Rozvojová 263, 165 02 Prague 6, Czech Republic.
Sex Plant Reprod. 2012 Mar;25(1):39-60. doi: 10.1007/s00497-011-0178-8. Epub 2011 Nov 20.
Male gametophyte development leading to the formation of a mature pollen grain is precisely controlled at various levels, including transcriptional, post-transcriptional and post-translational, during its whole progression. Transcriptomic studies exploiting genome-wide microarray technologies revealed the uniqueness of pollen transcriptome and the dynamics of early and late successive global gene expression programs. However, the knowledge of transcription regulation is still very limited. In this study, we focused on the identification of pollen-expressed transcription factor (TF) genes involved in the regulation of male gametophyte development. To achieve this, the reverse genetic approach was used. Seventy-four T-DNA insertion lines were screened, representing 49 genes of 21 TF families active in either early or late pollen development. In the screen, ten phenotype categories were distinguished, affecting various structural or functional aspects, including pollen abortion, presence of inclusions, variable pollen grain size, disrupted cell wall structure, cell cycle defects, and male germ unit organization. Thirteen lines were not confirmed to contain the T-DNA insertion. Among 61 confirmed lines, about half (29 lines) showed strong phenotypic changes (i.e., ≥ 25% aberrant pollen) including four lines that produced a remarkably high proportion (70-100%) of disturbed pollen. However, the remaining 32 lines exhibited mild defects or resembled wild-type appearance. There was no significant bias toward any phenotype category among early and late TF genes, nor, interestingly, within individual TF families. Presented results have a potential to serve as a basal information resource for future research on the importance of respective TFs in male gametophyte development.
雄性配子体发育直至形成成熟花粉粒的过程在各个层面都受到精确调控,包括转录、转录后和翻译后水平,贯穿其整个进程。利用全基因组微阵列技术进行的转录组学研究揭示了花粉转录组的独特性以及早期和晚期连续的全局基因表达程序的动态变化。然而,转录调控方面的知识仍然非常有限。在本研究中,我们专注于鉴定参与雄性配子体发育调控的花粉表达转录因子(TF)基因。为实现这一目标,我们采用了反向遗传学方法。筛选了74个T-DNA插入系,代表了21个TF家族的49个基因,这些基因在花粉发育的早期或晚期发挥作用。在筛选过程中,区分出了十种表型类别,影响各种结构或功能方面,包括花粉败育、内含物的存在、花粉粒大小可变、细胞壁结构破坏、细胞周期缺陷以及雄配子体单位组织。有13个系未被确认含有T-DNA插入。在61个确认的系中,约一半(29个系)表现出强烈的表型变化(即≥25%的异常花粉),其中四个系产生了极高比例(70-100%)的异常花粉。然而,其余32个系表现出轻微缺陷或类似野生型外观。在早期和晚期TF基因之间,以及有趣的是,在单个TF家族内部,对任何表型类别都没有明显的偏向性。所呈现的结果有可能作为未来研究各个TF在雄性配子体发育中的重要性的基础信息资源。