Maruyama Kouichi, Yasumasu Shigeki, Iuchi Ichiro
Life Science Institute, Sophia University, 7-1 Kioi-cho, Chiyoda-ku, Tokyo 102-8554, Japan.
Mech Dev. 2004 Jul;121(7-8):753-69. doi: 10.1016/j.mod.2004.03.035.
Recently we cloned two globin gene clusters from the genome of medaka (Oryzias latipes): one designated the embryonic globin gene cluster (E1; (5')alpha0(3')-(3')beta1(5')-(5')alpha1(3')-(5')beta2(3')-(5')alpha2(3')-(3')alpha3(5')-(5')beta3(3')-(3')beta4(5')-(5')alpha4(3')-(3')psialpha(5')-(5')psibeta(3')) and the other the adult globin gene cluster (A1; (3')ad.alpha1(5')-(5')ad.beta1(3')-(3')ad.alpha2(5')). The E1 and A1 clusters map to linkage groups 8 and 19, respectively. The genes beta1/alpha1, alpha3/beta3, beta4/alpha4, psialpha/psibeta and ad.alpha1/ad.beta1 are organized in head-to-head orientation with respect to transcriptional polarity. The genes alpha0, alpha1 and alpha2 are arranged in tandem with the same orientation. The results suggest that a variety of events occurred in globin gene evolution such as chromosomal translocation, duplication of alpha/beta-paired genes, tandem duplication of single alpha genes and the transformation of one pair of alpha/beta-paired genes into pseudogenes (psialpha/psibeta). Amino acid sequences predicted from the genes were compared with those of 42 alpha and 55 beta teleostean globins using the neighbor-joining or maximum likelihood methods. The phylogenetic trees that were generated classified the teleostean globins into at least four groups, tentatively named 'Embryonic Hb Group (I)', 'Notothenioid Major Adult Hb Group (II)', 'Anodic Adult Hb Group (III)' and 'Cathodic Adult Hb Group (IV)'. The medaka genes alpha0, beta1, alpha1, alpha2, alpha3, beta3, beta4 and alpha4 belong to group I, and ad.alpha1 and ad.beta1 to group II. Further analysis suggests that psialpha/psibeta and beta2/ad.alpha2 belong to groups III and IV, respectively. Thus, globin genes in the medaka probably were diversified from four ancestral genes, one for each group. On the basis of the gene comparisons, we present a hypothetical pathway for globin gene evolution in the medaka.
最近,我们从青鳉(Oryzias latipes)的基因组中克隆了两个珠蛋白基因簇:一个被命名为胚胎珠蛋白基因簇(E1;(5')α0(3')-(3')β1(5')-(5')α1(3')-(5')β2(3')-(5')α2(3')-(3')α3(5')-(5')β3(3')-(3')β4(5')-(5')α4(3')-(3')ψα(5')-(5')ψβ(3')),另一个为成体珠蛋白基因簇(A1;(3')ad.α1(5')-(5')ad.β1(3')-(3')ad.α2(5'))。E1和A1基因簇分别定位于连锁群8和19。β1/α1、α3/β3、β4/α4、ψα/ψβ和ad.α1/ad.β1基因相对于转录极性以头对头的方向排列。α0、α1和α2基因以相同方向串联排列。结果表明,在珠蛋白基因进化过程中发生了多种事件,如染色体易位、α/β配对基因的复制、单个α基因的串联复制以及一对α/β配对基因向假基因(ψα/ψβ)的转变。使用邻接法或最大似然法将从这些基因预测得到的氨基酸序列与42种α和55种β硬骨鱼珠蛋白的序列进行了比较。生成的系统发育树将硬骨鱼珠蛋白至少分为四组,暂命名为“胚胎血红蛋白组(I)”、“南极鱼主要成体血红蛋白组(II)”、“阳极成体血红蛋白组(III)”和“阴极成体血红蛋白组(IV)”。青鳉的α0、β1、α1、α2、α3、β3、β4和α4基因属于I组,ad.α1和ad.β1属于II组。进一步分析表明,ψα/ψβ和β2/ad.α2分别属于III组和IV组。因此,青鳉中的珠蛋白基因可能从四个祖先基因分化而来,每组一个。基于基因比较,我们提出了青鳉珠蛋白基因进化的假设途径。