Biochemical and Biophysical Research Communications, Vol.293, No.1, 327-331, 2002
Conserved physical linkage of GnRH-R and RBM8 in the medaka and human genomes
Candidate genes for human type 11 gonadotropin-releasing hormone receptor (GnRH-R11) reside on two separate loci, 1q12-q21 and 14q21-23, yet neither locus generates functional GnRH-RII, Instead, their opposite DNA strands encode functional RNA-binding motif protein 8 (RBM8s), which is also encoded by another locus, 5q13-q14. To elucidate the mechanism through which such multiple human GnRH-RII/RBM8 loci arose, here we have defined an RBM8 locus in a comparative model species, the medaka Oryzias latipes. The medaka RBM8, which exists as a single copy gene, is linked to, but does not overlap with, GnRH-R2 on linkage group (LG) 16, demonstrating the ancient origin of the physical linkage between GnRH-R and RBM8. The medaka LG 16 contains orthologous segments to the human chromosome I and therefore the 1q12-q21 locus would be an originating human GnRH-RII/RBM8 segment. Furthermore, like the human RBM8s on 1q12-q21 and 5q13-q14 but not that on 14q21-q23, the medaka RBM8 is a multiexon gene, indicating that the 14q21-q23 and 5q13-q14 loci were generated by retrotransposition and segmental genomic duplication, respectively, of the originating 1q12-q21 locus. (C) 2002 Elsevier Science (USA). All rights reserved.
Keywords:gonadotropin-releasing hormone receptor (GnRH-R);RNA-binding motif protein 8 (RBM8);linkage group;chromosome;mapping;medaka