Higgs Henry N, Peterson Kevin J
Department of Biochemistry, Dartmouth Medical School, Hanover, NH 03755, USA.
Mol Biol Cell. 2005 Jan;16(1):1-13. doi: 10.1091/mbc.e04-07-0565. Epub 2004 Oct 27.
Formin proteins are key regulators of eukaryotic actin filament assembly and elongation, and many species possess multiple formin isoforms. A nomenclature system based on fundamental features would be desirable, to aid the rapid identification and characterization of novel formins. In this article, we attempt to systematize the formin family by performing phylogenetic analyses of the formin homology 2 (FH2) domain, an independently folding region common to all formins, which alone can influence actin dynamics. Through database searches, we identify 101 FH2 domains from 26 eukaryotic species, including 15 in mice. Sequence alignments reveal a highly conserved yeast-specific insert in the "knob loop" region of the FH2 domain, with unknown functional consequences. Phylogenetic analysis using minimum evolution (ME), maximum parsimony (MP), and maximum likelihood (ML) algorithms strongly supports the existence of seven metazoan groups. Yeast FH2 domains segregate from all other eukaryotes, including metazoans, other fungi, plants, and protists. Sequence comparisons of non-FH2 regions support relationships between three metazoan groups (Dia, DAAM, and FRL) and examine previously identified coiled-coil and Diaphanous auto-regulatory domain sequences. This analysis allows for a formin nomenclature system based on sequence relationships, as well as suggesting strategies for the determination of biochemical and cellular activities of these proteins.
成束蛋白是真核生物肌动蛋白丝组装和延长的关键调节因子,许多物种都拥有多种成束蛋白亚型。基于基本特征的命名系统将有助于快速识别和表征新型成束蛋白。在本文中,我们试图通过对成束蛋白同源性2(FH2)结构域进行系统发育分析来使成束蛋白家族系统化,FH2结构域是所有成束蛋白共有的一个独立折叠区域,其自身就能影响肌动蛋白动力学。通过数据库搜索,我们从26种真核生物中鉴定出101个FH2结构域,其中包括小鼠中的15个。序列比对揭示了FH2结构域“旋钮环”区域中一个高度保守的酵母特异性插入片段,其功能后果未知。使用最小进化(ME)、最大简约(MP)和最大似然(ML)算法进行的系统发育分析有力地支持了七个后生动物组的存在。酵母FH2结构域与所有其他真核生物分离,包括后生动物、其他真菌、植物和原生生物。非FH2区域的序列比较支持了三个后生动物组(Dia、DAAM和FRL)之间的关系,并检查了先前鉴定的卷曲螺旋和透明自调节结构域序列。该分析允许基于序列关系建立一个成束蛋白命名系统,并提出确定这些蛋白质生化和细胞活性的策略。