Experimental Farm, National Institute of Genetics, Mishima, Shizuoka, 411-8540, Japan.
Department of Genetics, School of Life Science, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka, 411-8540, Japan.
Plant Mol Biol. 2015 Oct;89(3):293-307. doi: 10.1007/s11103-015-0369-z. Epub 2015 Aug 30.
Post-transcriptional gene regulation by RNA recognition motif (RRM) proteins through binding to cis-elements in the 3'-untranslated region (3'-UTR) is widely used in eukaryotes to complete various biological processes. Rice MEIOSIS ARRESTED AT LEPTOTENE2 (MEL2) is the RRM protein that functions in the transition to meiosis in proper timing. The MEL2 RRM preferentially associated with the U-rich RNA consensus, UUAGUU[U/A][U/G][A/U/G]U, dependently on sequences and proportionally to MEL2 protein amounts in vitro. The consensus sequences were located in the putative looped structures of the RNA ligand. A genome-wide survey revealed a tendency of MEL2-binding consensus appearing in 3'-UTR of rice genes. Of 249 genes that conserved the consensus in their 3'-UTR, 13 genes spatiotemporally co-expressed with MEL2 in meiotic flowers, and included several genes whose function was supposed in meiosis; such as Replication protein A and OsMADS3. The proteome analysis revealed that the amounts of small ubiquitin-related modifier-like protein and eukaryotic translation initiation factor3-like protein were dramatically altered in mel2 mutant anthers. Taken together with transcriptome and gene ontology results, we propose that the rice MEL2 is involved in the translational regulation of key meiotic genes on 3'-UTRs to achieve the faithful transition of germ cells to meiosis.
RNA 识别基序 (RRM) 蛋白通过与 3'非翻译区 (3'UTR) 中的顺式元件结合来进行转录后基因调控,这在真核生物中被广泛用于完成各种生物过程。水稻减数分裂前期 arrest2 (MEL2) 是一种 RRM 蛋白,它在减数分裂的适当时间发挥作用。MEL2 的 RRM 优先与富含 U 的 RNA 共识序列 UUAGUU[U/A][U/G][A/U/G]U 结合,这取决于序列和 MEL2 蛋白在体外的含量。共识序列位于 RNA 配体的推定环结构中。全基因组调查显示,MEL2 结合的共识序列在水稻基因的 3'UTR 中出现的趋势。在其 3'UTR 中保守共识序列的 249 个基因中,有 13 个基因在减数分裂花中与 MEL2 时空共表达,其中包括几个被认为在减数分裂中起作用的基因,如复制蛋白 A 和 OsMADS3。蛋白质组分析显示,mel2 突变体花药中小泛素相关修饰蛋白和真核翻译起始因子 3 样蛋白的含量发生了显著变化。综合转录组和基因本体论的结果,我们提出水稻 MEL2 参与关键减数分裂基因在 3'UTR 上的翻译调控,以实现生殖细胞向减数分裂的忠实转变。