TY - JOUR
T1 - Regulation of lens fiber cell differentiation by transcription factor c- Maf
AU - Kawauchi, Shimako
AU - Takahashi, Satoru
AU - Nakajima, Osamu
AU - Ogino, Hajime
AU - Morita, Masanobu
AU - Nishizawa, Makoto
AU - Yasuda, Kunio
AU - Yamamoto, Masayuki
PY - 1999/7/2
Y1 - 1999/7/2
N2 - To elucidate the regulatory mechanisms underlying lens development, we searched for members of the large Maf family, which are expressed in the mouse lens, and found three, c-Maf, MafB, and Nrl. Of these, the earliest factor expressed in the lens was c-Maf. The expression of c-Maf was most prominent in lens fiber cells and persisted throughout lens development. To examine the functional contribution of c-Maf to lens development, we isolated genomic clones encompassing the murine c-maf gene and carried out its targeted disruption. Insertion of the β-galactosidase (lacZ) gene into the c-maf locus allowed visualization of c-Maf accumulation in heterozygous mutant mice by staining for LacZ activity. Homozygous mutant embryos and newborns lacked normal lenses. Histological examination of these mice revealed defective differentiation of lens fiber cells. The expression of crystallin genes was severely impaired in the c-maf-null mutant mouse lens. These results demonstrate that c-Maf is an indispensable regulator of lens differentiation during murine development.
AB - To elucidate the regulatory mechanisms underlying lens development, we searched for members of the large Maf family, which are expressed in the mouse lens, and found three, c-Maf, MafB, and Nrl. Of these, the earliest factor expressed in the lens was c-Maf. The expression of c-Maf was most prominent in lens fiber cells and persisted throughout lens development. To examine the functional contribution of c-Maf to lens development, we isolated genomic clones encompassing the murine c-maf gene and carried out its targeted disruption. Insertion of the β-galactosidase (lacZ) gene into the c-maf locus allowed visualization of c-Maf accumulation in heterozygous mutant mice by staining for LacZ activity. Homozygous mutant embryos and newborns lacked normal lenses. Histological examination of these mice revealed defective differentiation of lens fiber cells. The expression of crystallin genes was severely impaired in the c-maf-null mutant mouse lens. These results demonstrate that c-Maf is an indispensable regulator of lens differentiation during murine development.
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U2 - 10.1074/jbc.274.27.19254
DO - 10.1074/jbc.274.27.19254
M3 - Article
C2 - 10383433
AN - SCOPUS:0033516565
SN - 0021-9258
VL - 274
SP - 19254
EP - 19260
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 27
ER -