期刊
MECHANISMS OF DEVELOPMENT
卷 120, 期 2, 页码 241-252出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/S0925-4773(02)00416-1
关键词
Alx3; aristaless-related gene; paired-type homeobox gene; OAR (aristaless)-domain; gain of function mutant; mouse embryogenesis; transcriptional activation; DNA-protein interaction; Meckel's cartilage; polydactyly; skeletal development; vertebrae
Aristaless-related genes encode a structurally defined group of homeoproteins that share a C-terminal stretch of amino acids known as the OAR- or aristaless domain. Many aristaless-related genes have been linked to major developmental functions, but the function of the aristaless domain itself is poorly understood. Expression and functional studies have shown that a subgroup of these genes, including Prx1, Prx2, Alx3, Alx4 and Cart1, is essential for correct morphogenesis of the limbs and cranium. We now demonstrate the function of the aristaless domain in vivo by ectopically expressing normal and mutated forms of Cart1 and Alx3. Ectopic expression of Cart1 in transgenic mice does not disturb development, whereas expression of a Cart1 form from which the aristaless domain has been deleted results in severe cranial and vertebral malformations. The Alx3 protein contains a divergent aristaless domain that appears not to be functional, as ectopic expression of Alx3 results in an altered phenotype irrespective of the presence of this aristaless domain. Linking the Cart1 aristaless domain to Alx3 extinguishes teratogenicity. We show that, at the molecular level, the most important consequence of deleting the aristaless domain is increased DNA binding to its palindromic target sequence. This demonstrates that the aristaless domain functions as an intra-molecular switch to contain the activity of the transcription factor that it is part of. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
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