The two functional keratin 6 genes of mouse are differentially regulated and evolved independently from their human orthologs

被引:77
作者
Takahashi, K
Yan, B
Yamanishi, K
Imamura, S
Coulombe, PA
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD 21205 USA
[3] Kyoto Univ, Grad Sch Med, Dept Dermatol, Kyoto 606, Japan
[4] Kyoto Prefectural Univ Med, Dept Dermatol, Kyoto, Japan
关键词
D O I
10.1006/geno.1998.5476
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The type II keratin 6 (K6) features a complex expression pattern, with a constitutive component in a subset of stratified epithelia and an inducible component following injury and other types of acute challenges. Multiple genes encoding highly related K6 isoforms have been described for human and bovine, a unique feature among mammalian keratin genes. Here we report on the cloning and characterization of two functional genes and their cDNAs encoding the K6 isoforms in mouse and two related pseudogenes. A systematic comparison of the mouse and human K6 genes suggests that they evolved independently after these species diverged. The mK6 alpha and mK6 beta genes are organized in tandem with the same transcriptional orientation in the mouse genome. Similar to the human isoforms, the coding sequences for mK6 alpha and mK6 beta isoforms show similar to 95% identity. The two mouse K6 genes are differentially regulated at the mRNA level in several stratified epithelia. The mK6 alpha isoform mRNA clearly predominates in intact trunk skin of adult mice, where it is restricted to the outer root sheath of hair follicles. Both mRNAs are induced in epidermis and proximal hair follicles as early as 1 h following acute injury or topical application of phorbol esters and subsequently increase to a comparable extent but with different kinetics. These novel findings have important implications for the evolution, regulation, and function of K6 genes in mammalian species. (C) 1998 Academic Press.
引用
收藏
页码:170 / 183
页数:14
相关论文
共 50 条
[41]   USE OF MONOSPECIFIC ANTISERA AND CRNA PROBES TO LOCALIZE THE MAJOR CHANGES IN KERATIN EXPRESSION DURING NORMAL AND ABNORMAL EPIDERMAL DIFFERENTIATION [J].
STOLER, A ;
KOPAN, R ;
DUVIC, M ;
FUCHS, E .
JOURNAL OF CELL BIOLOGY, 1988, 107 (02) :427-446
[42]   A transgenic mouse model with an inducible skin blistering disease phenotype [J].
Takahashi, K ;
Coulombe, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14776-14781
[43]   Defining a region of the human keratin 6a gene that confers inducible expression in stratified epithelia of transgenic mice [J].
Takahashi, K ;
Coulombe, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (18) :11979-11985
[44]   CLONING AND CHARACTERIZATION OF MULTIPLE HUMAN GENES AND CDNAS ENCODING HIGHLY RELATED TYPE-II KERATIN-6 ISOFORMS [J].
TAKAHASHI, K ;
PALADINI, RD ;
COULOMBE, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (31) :18581-18592
[45]   THE SEQUENCE OF A TYPE-II KERATIN GENE EXPRESSED IN HUMAN-SKIN - CONSERVATION OF STRUCTURE AMONG ALL INTERMEDIATE FILAMENT GENES [J].
TYNER, AL ;
EICHMAN, MJ ;
FUCHS, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (14) :4683-4687
[46]   EVIDENCE FOR POSTTRANSCRIPTIONAL REGULATION OF THE KERATINS EXPRESSED DURING HYPERPROLIFERATION AND MALIGNANT TRANSFORMATION IN HUMAN-EPIDERMIS [J].
TYNER, AL ;
FUCHS, E .
JOURNAL OF CELL BIOLOGY, 1986, 103 (05) :1945-1955
[47]   A proline residue in the α-helical rod domain of type I keratin 16 destabilizes keratin heterotetramers [J].
Wawersik, M ;
Paladini, RD ;
Noensie, E ;
Coulombe, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32557-32565
[48]   MONOCLONAL-ANTIBODY ANALYSIS OF KERATIN EXPRESSION IN EPIDERMAL DISEASES - A 48- AND 56-KDALTON KERATIN AS MOLECULAR MARKERS FOR HYPERPROLIFERATIVE KERATINOCYTES [J].
WEISS, RA ;
EICHNER, R ;
SUN, TT .
JOURNAL OF CELL BIOLOGY, 1984, 98 (04) :1397-1406
[49]   Activation of the human transglutaminase 1 promoter in transgenic mice: terminal differentiation-specific expression of the TGM1-lacZ transgene in keratinized stratified squamous epithelia [J].
Yamada, K ;
Matsuki, M ;
Morishima, Y ;
Ueda, E ;
Tabata, K ;
Yasuno, H ;
Suzuki, M ;
Yamanishi, K .
HUMAN MOLECULAR GENETICS, 1997, 6 (13) :2223-2231
[50]   ORGANIZATION OF THE HUMAN KERATIN TYPE-II GENE-CLUSTER AT 12Q13 [J].
YOON, SJ ;
LEBLANCSTRACESKI, J ;
WARD, D ;
KRAUTER, K ;
KUCHERLAPATI, R .
GENOMICS, 1994, 24 (03) :502-508