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拟南芥和水稻花粉成熟过程中 MIKC*-Type MADS 盒基因的功能保守性。

Functional conservation of MIKC*-Type MADS box genes in Arabidopsis and rice pollen maturation.

机构信息

Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.

出版信息

Plant Cell. 2013 Apr;25(4):1288-303. doi: 10.1105/tpc.113.110049. Epub 2013 Apr 23.

Abstract

There are two groups of MADS intervening keratin-like and C-terminal (MIKC)-type MADS box genes, MIKC(C) type and MIKC* type. In seed plants, the MIKC(C) type shows considerable diversity, but the MIKC* type has only two subgroups, P- and S-clade, which show conserved expression in the gametophyte. To examine the functional conservation of MIKC*-type genes, we characterized all three rice (Oryza sativa) MIKC*-type genes. All three genes are specifically expressed late in pollen development. The single knockdown or knockout lines, respectively, of the S-clade MADS62 and MADS63 did not show a mutant phenotype, but lines in which both S-clade genes were affected showed severe defects in pollen maturation and germination, as did knockdown lines of MADS68, the only P-clade gene in rice. The rice MIKC*-type proteins form strong heterodimeric complexes solely with partners from the other subclade; these complexes specifically bind to N10-type C-A-rich-G-boxes in vitro and regulate downstream gene expression by binding to N10-type promoter motifs. The rice MIKC* genes have a much lower degree of functional redundancy than the Arabidopsis thaliana MIKC* genes. Nevertheless, our data indicate that the function of heterodimeric MIKC*-type protein complexes in pollen development has been conserved since the divergence of monocots and eudicots, roughly 150 million years ago.

摘要

有两组 MADS intervening keratin-like 和 C 末端(MIKC)-型 MADS 框基因,MIKC(C) 型和 MIKC* 型。在种子植物中,MIKC(C) 型表现出相当大的多样性,但 MIKC* 型只有两个亚组,P-和 S 族,在配子体中表现出保守的表达。为了研究 MIKC*-型基因的功能保守性,我们对三种水稻(Oryza sativa)MIKC*-型基因进行了特征分析。这三个基因都在花粉发育后期特异性表达。分别敲低或敲除 S 族 MADS62 和 MADS63 的单基因,不会出现突变表型,但同时影响这两个 S 族基因的敲除系表现出花粉成熟和萌发的严重缺陷,水稻中唯一的 P 族基因 MADS68 的敲低系也是如此。水稻 MIKC*-型蛋白仅与来自另一个亚族的伙伴形成强异源二聚体复合物;这些复合物在体外特异性结合 N10 型 C-A 丰富-G 盒,并通过结合 N10 型启动子基序调节下游基因表达。与拟南芥的 MIKC* 基因相比,水稻的 MIKC* 基因的功能冗余程度要低得多。然而,我们的数据表明,异源二聚体 MIKC*-型蛋白复合物在花粉发育中的功能自单子叶植物和双子叶植物分化以来就已经保守,大约在 1.5 亿年前。

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