Rogers M A, Langbein L, Praetzel S, Moll I, Krieg T, Winter H, Schweizer J
Division of Tumor Cell Regulation, German Cancer Research Center, Heidelberg, Germany.
Differentiation. 1997 Feb;61(3):187-94. doi: 10.1046/j.1432-0436.1997.6130187.x.
As part of a program designed to characterize human hair keratin genes and their expression, we present the cDNA sequences and deduced amino acid sequences of three type-II hair keratins hHb3, hHb5, and hHb6, which by virtue of their amino acid homologies are the orthologs of the previously described sheep wool keratins, K2.10, K2.12, and K.211 [29]. Amino acid sequences comparisons of these keratins, including the previously characterized human K2.9 ortholog hHb1, show extreme conservation not only in the alpha-helices but also in the aminoterminal and proximal carboxyterminal domains. They also demonstrate higher sequence relationships between hHb1, hHb3, and hHb6 as compared to hHb5, which exhibits chain-specific sequences in both the head and tail domains. In situ hybridization studies using specific 3'-probes for the four type-II hair keratins reveal sequential patterns of gene expression in human anagen follicles. Remarkably the onset of hHb5 mRNA synthesis occurs immediately above a small population of matrix cells at the base of the hair bulb and the trichocytes lining the dermal papilla. hHb5 mRNA synthesis extends upward through the matrix and ends in the lower part of the cortex of the hair shaft. In contrast, both hHb1 and hHb3 mRNA synthesis begins simultaneously in the cortex 10-15 cell layers above the apex of the dermal papilla, thus partially overlapping that of hHb5 but continuing to a point well beyond hHb5 in the upper cortex. Synthesis of hHb6 mRNA starts slightly higher than either hHb1 or hHb3 mRNA and proceeds much farther up into the keratogenous zone of the hair shaft. Our study demonstrates that the differentiation of human hair in terms of hair keratin expression begins much earlier than previously assumed, i.e. in lower matrix cells of the hair bulb. This early phase of hair differentiation is followed by a late cortical phase of terminal differentiation which comprises at least three type-II hair keratins in the zone of elongation and the keratogenous zone of the hair shaft.
作为一项旨在鉴定人类毛发角蛋白基因及其表达的研究计划的一部分,我们展示了三种II型毛发角蛋白hHb3、hHb5和hHb6的cDNA序列及推导的氨基酸序列,基于它们的氨基酸同源性,它们是先前描述的绵羊羊毛角蛋白K2.10、K2.12和K2.11的直系同源物[29]。这些角蛋白的氨基酸序列比较,包括先前已鉴定的人类K2.9直系同源物hHb1,不仅显示出α-螺旋中,而且在氨基末端和近端羧基末端结构域中都具有极高的保守性。与hHb5相比,hHb1、hHb3和hHb6之间也显示出更高的序列相关性,hHb5在头部和尾部结构域均表现出链特异性序列。使用针对四种II型毛发角蛋白的特异性3'-探针进行的原位杂交研究揭示了人类生长期毛囊中基因表达的顺序模式。值得注意的是,hHb5 mRNA合成起始于毛球底部一小群基质细胞以及围绕真皮乳头的毛母细胞上方。hHb5 mRNA合成向上延伸穿过基质并在毛干皮质的下部结束。相比之下,hHb1和hHb3 mRNA合成均在真皮乳头顶端上方10 - 15个细胞层的皮质中同时开始,因此部分与hHb5的合成重叠,但在上部皮质中继续延伸至远超hHb5的位置。hHb6 mRNA的合成起始位置略高于hHb1或hHb3 mRNA,并向上延伸至毛干的角质形成区更远的位置。我们的研究表明,就毛发角蛋白表达而言,人类毛发的分化比先前假设的要早得多,即在毛球的下部基质细胞中。毛发分化的这个早期阶段之后是晚期皮质终末分化阶段,在毛干的伸长区和角质形成区至少包括三种II型毛发角蛋白。