Kofuji Rumiko, Sumikawa Naomi, Yamasaki Misuzu, Kondo Kimihiko, Ueda Kunihiko, Ito Motomi, Hasebe Mitsuyasu
Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa, Japan.
Mol Biol Evol. 2003 Dec;20(12):1963-77. doi: 10.1093/molbev/msg216. Epub 2003 Aug 29.
MADS-box genes encode transcription factors involved in various important aspects of development and differentiation in land plants, metazoans, and other organisms. Three types of land plant MADS-box genes have been reported. MIKCC- and MIKC*-type genes both contain conserved MADS and K domains but have different exon/intron structures. M-type genes lack a K domain. Most MADS-box genes previously analyzed in land plants are expressed in the sporophyte (diploid plant body); few are expressed in the gametophyte (haploid plant body). Land plants are believed to have evolved from a gametophyte (haploid)-dominant ancestor without a multicellular sporophyte (diploid plant body); most genes expressed in the sporophyte probably originated from those used in the gametophyte during the evolution of land plants. To analyze the evolution and diversification of MADS-box genes in land plants, gametophytic MADS-box genes were screened using macroarray analyses for 105 MADS-box genes found in the Arabidopsis genome. Eight MADS-box genes were predominantly expressed in pollen, the male gametophyte; all but one of their expression patterns was confirmed by Northern analyses. Analyses of the exon/intron structure of these seven genes revealed that they included two MIKCC-type, one M-type, and four MIKC*-type MADS-box genes. Previously, MIKC*-type genes have been reported only from a moss and a club moss, and this is the first record in seed plants. These genes can be used to investigate the unknown ancestral functions of MADS-box genes in land plants. The macroarray analyses did not detect expression of 56 of 61 M-type MADS-box genes in any tissues examined. A phylogenetic tree including all three types of Arabidopsis MADS-box genes with representative genes from other organisms showed that M-type genes were polyphyletic and that their branch lengths were much longer than for the other genes. This finding suggests that most M-type genes are pseudogenes, although further experiments are necessary to confirm this possibility. Our global phylogenetic analyses of MADS-box genes did not support the previous classification of MADS-box genes into type I and II groups, based on smaller scale analyses. An evolutionary scenario for the evolution of MADS-box genes in land plants is discussed.
MADS-box基因编码参与陆地植物、后生动物和其他生物发育与分化各个重要方面的转录因子。已报道了三种类型的陆地植物MADS-box基因。MIKCC型和MIKC型基因都含有保守的MADS和K结构域,但具有不同的外显子/内含子结构。M型基因缺少K结构域。先前在陆地植物中分析的大多数MADS-box基因在孢子体(二倍体植物体)中表达;很少在配子体(单倍体植物体)中表达。陆地植物被认为是从没有多细胞孢子体(二倍体植物体)的配子体(单倍体)占主导的祖先进化而来;在陆地植物进化过程中,大多数在孢子体中表达的基因可能起源于那些在配子体中使用的基因。为了分析陆地植物中MADS-box基因的进化和多样化,利用宏阵列分析对拟南芥基因组中发现的105个MADS-box基因筛选配子体MADS-box基因。八个MADS-box基因主要在花粉(雄配子体)中表达;除一个外,它们的表达模式均通过Northern分析得到证实。对这七个基因的外显子/内含子结构分析表明,它们包括两个MIKCC型、一个M型和四个MIKC型MADS-box基因。此前,MIKC*型基因仅在一种苔藓和一种石松中被报道,这是在种子植物中的首次记录。这些基因可用于研究陆地植物中MADS-box基因未知的祖先功能。宏阵列分析未在任何检测的组织中检测到61个M型MADS-box基因中56个的表达。一个包含拟南芥所有三种类型MADS-box基因以及来自其他生物的代表性基因的系统发育树表明,M型基因是多系的,并且它们的分支长度比其他基因长得多。这一发现表明大多数M型基因是假基因,尽管需要进一步实验来证实这种可能性。我们对MADS-box基因的全局系统发育分析不支持基于较小规模分析将MADS-box基因分为I型和II型组的先前分类。本文讨论了陆地植物中MADS-box基因进化的一种演化情形。