RT Journal
A1 Babushok, Daria V.
A1 Ohshima, Kazuhiko
A1 Ostertag, Eric M.
A1 Chen, Xinsheng
A1 Wang, Yanfeng
A1 Mandal, Prabhat K.
A1 Okada, Norihiro
A1 Abrams, Charles S.
A1 Kazazian, Haig H.
T1 A novel testis ubiquitin-binding protein gene arose by exon shuffling in hominoids
JF Genome Research 
JO Genome Research 
YR 2007 
FD August 01 
VO 17 
IS 8 
SP 000 
OP 000 
DO 10.1101/gr.6252107 
UL http://genome.cshlp.org/content/early/2007/07/10/gr.6252107.abstract 
AB Most new genes arise by duplication of existing gene structures, after which relaxed selection on the new copy frequently leads to mutational inactivation of the duplicate; only rarely will a new gene with modified function emerge. Here we describe a unique mechanism of gene creation, whereby new combinations of functional domains are assembled at the RNA level from distinct genes, and the resulting chimera is then reverse transcribed and integrated into the genome by the L1 retrotransposon. We characterized a novel gene, which we termed S5a-like (S5aL), created by this mechanism from an intergenic transcript between the phosphatidylinositol-4-phosphate 5-kinase (PIP5K1A) and the 26S proteasome subunit (S5a) genes in a hominoid ancestor. S5aL is transcribed specifically in the testis both in humans and chimpanzees, and is post-transcriptionally repressed by independent mechanisms in these primate lineages. The S5aL gene encodes a chimeric protein combining the lipid kinase domain of PIP5K1A and the ubiquitin-binding motifs of S5a. Strong positive selection on S5aL led to its rapid divergence from the parental genes PIP5K1A and S5a, forming a chimeric protein with a distinct cellular localization and minimal lipid kinase activity, but significant affinity for cellular ubiquitinated proteins. S5aL is a tightly regulated, testis-specific novel ubiquitin-binding protein formed by an unusual exon-shuffling mechanism in hominoid primates and represents a key example of rapid evolution of a testis-specific gene.