 Open Access
Open AccessMouse Transgenesis Identifies Conserved Functional Enhancers and cis-Regulatory Motif in the Vertebrate LIM Homeobox Gene Lhx2 Locus
Author(s) - 
Alison Lee, 
Sydney Brenner, 
Byrappa Venkatesh
Publication year - 2011
Publication title - 
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0020088
Subject(s) - biology , enhancer , homeobox , genetics , locus (genetics) , gene , conserved sequence , transcription factor , peptide sequence
The vertebrate  Lhx2  is a member of the LIM homeobox family of transcription factors. It is essential for the normal development of the forebrain, eye, olfactory system and liver as well for the differentiation of lymphoid cells. However, despite the highly restricted spatio-temporal expression pattern of  Lhx2 , nothing is known about its transcriptional regulation. In mammals and chicken,  Crb2 ,  Dennd1a  and  Lhx2  constitute a conserved linkage block, while the intervening  Dennd1a  is lost in the fugu  Lhx2  locus. To identify functional enhancers of  Lhx2 , we predicted conserved noncoding elements (CNEs) in the human, mouse and fugu  Crb2 - Lhx2  loci and assayed their function in transgenic mouse at E11.5. Four of the eight CNE constructs tested functioned as tissue-specific enhancers in specific regions of the central nervous system and the dorsal root ganglia (DRG), recapitulating partial and overlapping expression patterns of  Lhx2  and  Crb2  genes. There was considerable overlap in the expression domains of the CNEs, which suggests that the CNEs are either redundant enhancers or regulating different genes in the locus. Using a large set of CNEs (810 CNEs) associated with transcription factor-encoding genes that express predominantly in the central nervous system, we predicted four over-represented 8-mer motifs that are likely to be associated with expression in the central nervous system. Mutation of one of them in a CNE that drove reporter expression in the neural tube and DRG abolished expression in both domains indicating that this motif is essential for expression in these domains. The failure of the four functional enhancers to recapitulate the complete expression pattern of  Lhx2  at E11.5 indicates that there must be other  Lhx2  enhancers that are either located outside the region investigated or divergent in mammals and fishes. Other approaches such as sequence comparison between multiple mammals are required to identify and characterize such enhancers.
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