TY - JOUR
T1 - The cDNA sequence of a human epidermal keratin
T2 - Divergence of sequence but conservation of structure among intermediate filament proteins
AU - Hanukoglu, Israel
AU - Fuchs, Elaine
N1 - Funding Information:
cility. I. H. is the recipient of an NIH postdoctoral fellowship. E. F. is a Searle Scholar and the recipient of a Research Career Development Award. This work was supported by a grant from NIH.
PY - 1982/11
Y1 - 1982/11
N2 - We have determined the DNA sequence of a cloned cDNA that is complementary to the mRNA for the 50 kilodalton (kd) human epidermal keratin. This provides the first amino acid sequence for a cytoskeletal keratin. Comparison of this sequence with those of other keratins reveals an evolutionary relationship between the cytoskeletal and the microfibrillar keratins, but shows no homology to matrix or feather keratins. The 50 kd keratin shares 28%-30% homology with partial sequences of other intermediate filament proteins, which suggests that keratins may be the most distantly related members of this class of fibrous proteins. Our computer analyses predict that the 50 kd keratin contains two long α-helical domains separated by a cluster of helix-inhibitory residues in the middle of the protein. These findings indicate that despite major sequence divergence among intermediate filament proteins, they retain sequences compatible with secondary structural features that appear to be common to all of them.
AB - We have determined the DNA sequence of a cloned cDNA that is complementary to the mRNA for the 50 kilodalton (kd) human epidermal keratin. This provides the first amino acid sequence for a cytoskeletal keratin. Comparison of this sequence with those of other keratins reveals an evolutionary relationship between the cytoskeletal and the microfibrillar keratins, but shows no homology to matrix or feather keratins. The 50 kd keratin shares 28%-30% homology with partial sequences of other intermediate filament proteins, which suggests that keratins may be the most distantly related members of this class of fibrous proteins. Our computer analyses predict that the 50 kd keratin contains two long α-helical domains separated by a cluster of helix-inhibitory residues in the middle of the protein. These findings indicate that despite major sequence divergence among intermediate filament proteins, they retain sequences compatible with secondary structural features that appear to be common to all of them.
UR - http://www.scopus.com/inward/record.url?scp=0020446742&partnerID=8YFLogxK
U2 - 10.1016/0092-8674(82)90424-X
DO - 10.1016/0092-8674(82)90424-X
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C2 - 6186381
AN - SCOPUS:0020446742
SN - 0092-8674
VL - 31
SP - 243
EP - 252
JO - Cell
JF - Cell
IS - 1
ER -