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MOLECULAR CHARACTERIZATION OF THE BODY SITE-SPECIFIC HUMAN EPIDERMAL CYTOKERATIN-9 - CDNA CLONING, AMINO-ACID-SEQUENCE, AND TISSUE-SPECIFICITY OF GENE-EXPRESSION
Author(s): LANGBEIN L, HEID HW, MOLL I, FRANKE WW
Source: DIFFERENTIATION    Volume: 55    Issue: 1    Pages: 57-71    Published: DEC 1993  
Times Cited: 79     References: 132     
Abstract: Differentiation of human plantar and palmar epidermis is characterized by the suprabasal synthesis of a major special intermediate-sized filament (IF) protein, the type I (acidic) cytokeratin 9 (CK 9). Using partial amino acid (aa) sequence information obtained by direct Edman sequencing of peptides resulting from proteolytic digestion of purified CK 9, we synthesized several redundant primers by 'back-translation'. Amplification by polymerase chain reaction (PCR) of cDNAs obtained by reverse transcription of mRNAs from human foot sole epidermis, including 5'-primer extension, resulted in multiple overlapping cDNA clones, from which the complete cDNA (2353 bp) could be constructed. This cDNA encoded the CK 9 polypeptide with a calculated molecular weight of 61987 and an isoelectric point at about pH 5.0. The aa sequence deduced from cDNA was verified in several parts by comparison with the peptide sequences and showed the typical structure of type I CKs, with a head (153 aa), an alpha-helical coiled-coilforming rod (306 aa), and a tail (163 aa) domain. The protein displayed the highest homology to human CK 10, not only in the highly conserved rod domain but also in large parts of the head and the tail domains. On the other hand, the aa sequence revealed some remarkable differences from CK 10 and other CKs, even in the most conserved segments of the rod domain. The nuclease digestion pattern seen on Southern blot analysis of human genomic DNA indicated the existence of a unique CK 9 gene.

Using CK 9-specific riboprobes for hybridization on Northern blots of RNAs from various epithelia, a mRNA of about 2.4 kb in length could be identified only in foot sole epidermis, and a weaker cross-hybridization signal was seen in RNA from bovine heel pad epidermis at about 2.0 kb. A large number of tissues and cell cultures were examined by PCR of mRNA-derived cDNAs, using CK 9-specific primers. But even with this very sensitive signal amplification, only palmar/plantar epidermis was found positive. By in situ hybridization and immunolocalization we further showed that CK 9 is only expressed in the suprabasal cell layers of this special epidermal tissue. We discuss the molecular properties of CK 9 and its cell type and body site specific expression in relation to the special differentiation of palmar/plantar epidermis and to diseases specific for this body site.

Document Type: Review
Language: English
Addresses:
1. GERMAN CANC RES CTR, DIV CELL BIOL, D-69120 HEIDELBERG, GERMANY
2. UNIV HEIDELBERG, MANNHEIM MED SCH, DEPT DERMATOL, D-68167 MANNHEIM, GERMANY
Publisher: SPRINGER VERLAG, 175 FIFTH AVE, NEW YORK, NY 10010
Subject Category: Cell Biology; Developmental Biology
IDS Number: MM581
ISSN: 0301-4681
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