Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b

被引:83
作者
Wojcik, SM
Longley, MA
Roop, DR
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Dermatol, Houston, TX 77030 USA
关键词
keratin; skin; tongue; hair follicle; pachyonychia congenita;
D O I
10.1083/jcb.200102079
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The murine genome is known to have two keratin 6 (K6) genes, mouse K6 (MK6)a and MK6b. These genes display a complex expression pattern with constitutive expression in the epithelia of oral mucosa, hair follicles, and nail beds. We generated mice deficient for both genes through embryonic stem cell technology. The majority of MK6a/b(-/-) mice die of starvation within the first two weeks of life. This is due to a localized disintegration of the dorsal tongue epithelium, which results in the build up of a plaque of cell debris that severely impairs feeding. However, similar to 25% of MK6a/b(-/-) mice survive to adulthood. Remarkably, the surviving MK6a/b(-/-) mice have normal hair and nails. To our surprise, we discovered MK6 staining both in the hair follicle and the nail bed of MK6a/b(-/-) mice, indicating the presence of a third MK6 gene. We cloned this previously unknown murine keratin gene and found it to be highly homologous to human K6hf, which is expressed in hair follicles. We therefore termed this gene MK6 hair follicle (MK6hf). The presence of MK6hf in the MK6a/b(-/-) follicles and nails offers an explanation for the absence of hair and nail defects in MK6a/b(-/-) animals.
引用
收藏
页码:619 / 630
页数:12
相关论文
共 46 条
[1]   COLORECTAL HYPERPLASIA AND INFLAMMATION IN KERATIN 8-DEFICIENT EVB/N MICE [J].
BARIBAULT, H ;
PENNER, J ;
IOZZO, RV ;
WILSONHEINER, M .
GENES & DEVELOPMENT, 1994, 8 (24) :2964-2973
[2]   MIDGESTATIONAL LETHALITY IN MICE LACKING KERATIN-8 [J].
BARIBAULT, H ;
PRICE, J ;
MIYAI, K ;
OSHIMA, RG .
GENES & DEVELOPMENT, 1993, 7 (7A) :1191-1202
[3]   A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis [J].
Bickenbach, JR ;
Longley, MA ;
Bundman, DS ;
Dominey, AM ;
Bowden, PE ;
Rothnagel, JA ;
Roop, DR .
DIFFERENTIATION, 1996, 61 (02) :129-139
[4]   DIFFERENTIALLY EXPRESSED BOVINE CYTOKERATIN GENES - ANALYSIS OF GENE LINKAGE AND EVOLUTIONARY CONSERVATION OF 5'-UPSTREAM SEQUENCES [J].
BLESSING, M ;
ZENTGRAF, H ;
JORCANO, JL .
EMBO JOURNAL, 1987, 6 (03) :567-575
[5]   MUTATION OF A TYPE-II KERATIN GENE (K6A) IN PACHYONYCHIA-CONGENITA [J].
BOWDEN, PE ;
HALEY, JL ;
KANSKY, A ;
ROTHNAGEL, JA ;
JONES, DO ;
TURNER, RJ .
NATURE GENETICS, 1995, 10 (03) :363-365
[6]   Identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2 [J].
Çelebi, JT ;
Tanzi, EL ;
Yao, YJ ;
Michael, EJ ;
Peacocke, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (05) :848-850
[7]  
Corden L D, 1996, Exp Dermatol, V5, P297, DOI 10.1111/j.1600-0625.1996.tb00133.x
[8]  
Covello SP, 1998, BRIT J DERMATOL, V139, P475
[9]   Pachyonychia congenita type 2: Keratin 17 mutation in a Japanese case [J].
Fujimoto, W ;
Nakanishi, G ;
Hirakawa, S ;
Nakanishi, T ;
Shimo, T ;
Takigawa, M ;
Arata, J .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1998, 38 (06) :1007-1009
[10]   THE COILED COIL OF INVITRO ASSEMBLED KERATIN FILAMENTS IS A HETERODIMER OF TYPE-I AND TYPE-II KERATINS - USE OF SITE-SPECIFIC MUTAGENESIS AND RECOMBINANT PROTEIN EXPRESSION [J].
HATZFELD, M ;
WEBER, K .
JOURNAL OF CELL BIOLOGY, 1990, 110 (04) :1199-1210