Rapid repetitive element-mediated expansion of piRNA clusters in mammalian evolution

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 106; no. 17; pp. 7079 - 7082
• Main Authors: Assis, Raquel, Kondrashov, Alexey S
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 28.04.2009; National Acad Sciences
• Subjects: Animals; Biochemistry; Biological Sciences; Cells; Chromosomes; Evolution; Evolution, Molecular; Genes; Genetic Variation - genetics; Genomes; Genomics; Humans; Mammals; Mice; Multigene Family - genetics; Proteins; Rats; Recombination, Genetic - genetics; Ribonucleic acid; RNA; RNA, Small Interfering - genetics; Rodents; Time Factors; Transposons
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.0900523106

Piwi-interacting RNAs (piRNAs) are [almost equal to]30 nucleotide noncoding RNAs that may be involved in transposon silencing in mammalian germline cells. Most piRNA sequences are found in a small number of genomic regions referred to as clusters, which range from 1 to hundreds of kilobases. We studied the evolution of 140 rodent piRNA clusters, 103 of which do not overlap protein-coding genes. Phylogenetic analysis revealed that 14 clusters were acquired after rat-mouse divergence and another 44 after rodent-primate divergence. Most clusters originated in a process analogous to the duplication of protein-coding genes by ectopic recombination, via insertions of long sequences that were mediated by flanking chromosome-specific repetitive elements (REs). Source sequences for such insertions are often located on the same chromosomes and also harbor clusters. The rate of piRNA cluster expansion is higher than that of any known gene family and, in contrast to other large gene families, there was not a single cluster loss. These observations suggest that piRNA cluster expansion is driven by positive selection, perhaps caused by the need to silence the ever-expanding repertoire of mammalian transposons.