Lingrel J B, Townes T M, Shapiro S G, Wernke S M, Liberator P A, Menon A G
Prog Clin Biol Res. 1985;191:67-79.
Goats switch their hemoglobins during development in a manner similar to humans and thus provide a useful model system for studying the control of hemoglobin synthesis. Initially, goats synthesize embryonic hemoglobin, zeta 2 epsilon 2, which is replaced by fetal hemoglobin, alpha 2 beta F 2, as erythropoiesis moves to the liver and bone marrow. At birth, the fetal hemoglobin is replaced by juvenile hemoglobin, alpha 2 beta C 2, which in turn is replaced by adult hemoglobin, alpha 2 beta A 2, during the first year of life. In order to understand these switches, we have cloned the alpha and beta globin loci of goats. The alpha globin locus is composed of three genes, an embryonic and two adult genes, zeta-I alpha-II alpha. The beta globin locus is composed of twelve genes arranged in the following order, epsilon I-epsilon II-psi beta X-beta C-epsilon III-epsilon IV-psi beta Z-beta A-epsilon V-epsilon VI-psi beta Y-beta F. Close inspection of the beta globin locus indicates that it has arisen from a triplication of a four-gene set, epsilon-epsilon-beta-beta. Interestingly, the fetal globin gene has originated from an adult beta globin gene rather than from a second position gene as it has in humans. The gene at the end of the first four gene set, beta C, is expressed during pre-adult life while the gene at the end of the second set is the adult beta A gene. The last gene of the third set, beta F, is expressed during fetal development. Because the beta C, beta A and beta F genes have arisen quite recently during evolution, they have very similar nucleotide sequences. It is reasonable to assume that the few differences which are seen are important in developmental control. As one approach to defining regions involved in the regulation of the beta A, beta C and beta F genes their chromatin structure at different times of development has been characterized. Both DNase I sensitivity and accessibility to restriction endonucleases have been employed. While the entire beta globin locus is more sensitive to DNase in erythroid than non-erythroid cells, specific regions such as the 5' end of the genes are more accessible in cells expressing that particular gene.
山羊在发育过程中切换血红蛋白的方式与人类相似,因此为研究血红蛋白合成的调控提供了一个有用的模型系统。最初,山羊合成胚胎血红蛋白ζ₂ε₂,随着红细胞生成转移到肝脏和骨髓,它会被胎儿血红蛋白α₂βF₂取代。出生时,胎儿血红蛋白被幼年血红蛋白α₂βC₂取代,而幼年血红蛋白在生命的第一年又会被成人血红蛋白α₂βA₂取代。为了理解这些转换,我们克隆了山羊的α和β珠蛋白基因座。α珠蛋白基因座由三个基因组成,一个胚胎基因和两个成人基因,即ζ-Iα-IIα。β珠蛋白基因座由十二个基因组成,排列顺序如下:εI-εII-ψβX-βC-εIII-εIV-ψβZ-βA-εV-εVI-ψβY-βF。仔细观察β珠蛋白基因座会发现它起源于一个四基因组ε-ε-β-β的三倍体。有趣的是,胎儿珠蛋白基因起源于成人β珠蛋白基因,而不是像人类那样起源于第二个位置的基因。第一个四基因组末尾的基因βC在成年前表达,而第二个组末尾的基因是成人βA基因。第三组的最后一个基因βF在胎儿发育期间表达。由于βC、βA和βF基因在进化过程中出现的时间相当近,它们具有非常相似的核苷酸序列。可以合理地假设,所观察到的少数差异在发育调控中很重要。作为定义参与βA、βC和βF基因调控区域的一种方法,已经对它们在不同发育阶段的染色质结构进行了表征。同时使用了DNase I敏感性和对限制性内切酶的可及性。虽然整个β珠蛋白基因座在红细胞系细胞中比非红细胞系细胞对DNase更敏感,但特定区域,如基因的5'端,在表达该特定基因的细胞中更容易接近。