Fuchs E
J Invest Dermatol. 1983 Jul;81(1 Suppl):141s-4s. doi: 10.1111/1523-1747.ep12540922.
The keratins are a family of proteins (Mr = 40-70 K) that form 8-nm intermediate filaments in the cytoplasm of most vertebrate epithelial cells. Each epithelial cell expresses its own subset of keratins, which consists of about 2 to 5 polypeptides. In epidermis, the keratins are especially abundant, comprising 30 to 85 percent of the total protein of these cells. Four major keratins (Mr = 46, 50, 56, and 58 K) are expressed in the basal cells, whereas the larger keratins (60-70 K) are found only in differentiating epidermal cells. We have shown that in human epidermis there are multiple mRNAs for the keratins. These RNAs can be grouped into two distinct classes as judged by their ability to hybridize to one of two separate classes of cloned keratin cDNA sequences. Each of these two classes of sequences is encoded by a multigene family of about 10 genes each, and these two families are coordinately conserved throughout vertebrate evolution [21]. Recently, we have determined the DNA sequence of a cloned cDNA insert that is complementary to greater than 90 percent of the coding region for the 50 K keratin and which shares homology with 46 K keratin mRNA [13]. A comparison of the predicted amino acid sequence of this cytoskeletal keratin with partial sequences of keratins of epidermal appendages, e.g., wool, shows that there is a distinct relation with the fibrous keratins of wool, but little or no relation with the matrix keratins. A comparison of the 50 K keratin sequence with the partial sequences known for other intermediate-filament proteins indicates that the keratins may be the most distantly related of this class of 80- to 100-A filamentous proteins. This is in contrast to the actins and tubulins, which are highly conserved components of vertebrate cytoskeletons. The wide flexibility in the amino acid sequence of intermediate filament proteins suggests that these proteins have evolved to meet subtly different requirements in the cytoskeletal architecture.
角蛋白是一族蛋白质(分子量为40 - 70K),在大多数脊椎动物上皮细胞的细胞质中形成8纳米的中间丝。每个上皮细胞表达其自身的角蛋白亚群,该亚群由约2至5种多肽组成。在表皮中,角蛋白尤其丰富,占这些细胞总蛋白的30%至85%。四种主要角蛋白(分子量为46K、50K、56K和58K)在基底细胞中表达,而较大的角蛋白(60 - 70K)仅在分化的表皮细胞中发现。我们已经表明,在人类表皮中存在角蛋白的多种mRNA。根据它们与两类不同的克隆角蛋白cDNA序列之一杂交的能力判断,这些RNA可分为两个不同的类别。这两类序列中的每一类都由一个约含10个基因的多基因家族编码,并且这两个家族在整个脊椎动物进化过程中是协同保守的[21]。最近,我们确定了一个克隆的cDNA插入片段的DNA序列,该片段与50K角蛋白编码区的90%以上互补,并且与46K角蛋白mRNA具有同源性[13]。将这种细胞骨架角蛋白的预测氨基酸序列与表皮附属器(如羊毛)角蛋白的部分序列进行比较,结果表明它与羊毛的纤维角蛋白有明显关系,但与基质角蛋白几乎没有关系。将50K角蛋白序列与其他中间丝蛋白的已知部分序列进行比较表明,角蛋白可能是这类80至100埃丝状蛋白中关系最疏远的。这与肌动蛋白和微管蛋白形成对比,它们是脊椎动物细胞骨架中高度保守的成分。中间丝蛋白氨基酸序列的广泛灵活性表明,这些蛋白质已经进化以满足细胞骨架结构中细微不同的需求。