Insertional mutation of the mouse Msx1 homeobox gene by an nlacZ reporter gene.

Abstract:

:We have generated a null allele of the mouse Msx1 homeobox gene by insertion of an nlacZ reporter gene into its homeobox. The sensitivity of beta-galactosidase detection permitted us to reveal novel aspects of Msx1 gene expression in heterozygous embryos, in particular in ectoderm and mesoderm during gastrulation, and in migrating neural crest cells. Homozygous mutant mice die at birth with facial defects (see Satokata, I. and Maas, R. (1994) Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat. Genet. 6, 348-356). To investigate the reason for this limited phenotype, we compared the pattern of Msx1 expression with that of the closely related Msx2 gene in wild type embryos and in Msx1-/- mutants. Notably, whereas the expression of Msx1 and Msx2 overlap in the developing limb, this is not the case in the facial regions most affected in the mutant.

journal_name

Mech Dev

authors

Houzelstein D,Cohen A,Buckingham ME,Robert B

doi

10.1016/s0925-4773(97)00065-8

subject

Has Abstract

pub_date

1997-07-01 00:00:00

pages

123-33

issue

1-2

eissn

0925-4773

issn

1872-6356

pii

S0925-4773(97)00065-8

journal_volume

65

pub_type

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