Genomic analysis of the nuclear receptor family: New insights into structure, regulation, and evolution from the rat genome

被引:162
|
作者
Zhang, ZD
Burch, PE
Cooney, AJ
Lanz, RB
Pereira, FA
Wu, JQ
Gibbs, RA
Weinstock, G
Wheeler, DA [1 ]
机构
[1] Baylor Coll Med, Human Genome Sequencing Ctr, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Baylor Coll Med, Huffington Ctr Aging, Dept Otolaryngol, Houston, TX 77030 USA
[4] Univ Texas, Sch Med, Dept Microbiol & Mol Genet, Houston, TX 77225 USA
关键词
D O I
10.1101/gr.2160004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Completion of the Rattus norvegicus genome sequence enabled a global inventory and analysis of the nuclear receptors (NRs) in three mammalian species. Forty-nine NR members were found in mouse, 48 in human. Forty-seven were found in the rat, with gaps at the locations expected for the other two. Pairwise comparisons of their distribution in rat, mouse, and human identified II syntenic NR gene blocks, including three small clusters of two or three closely related genes, each spanning 40 kb to 1700 kb. The exon structure of the ligand-binding domain suggests that exon shuffling has played a role in the evolution of this family. An invariant splice junction in all members of the NR family except LXRbeta Suggests a functional role for the intron. The ligand-binding domains of PXR and CAR are among the most divergent in the family. Their higher nucleotide Substitution rates may be related to the central role played by these two NRs in the metabolism of the foreign compounds and may have resulted from limited positive selection.
引用
收藏
页码:580 / 590
页数:11
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