TY - JOUR
T1 - Adaptive regulation of testis gene expression and control of male fertility by the drosophila harpin RNA pathway
AU - Wen, Jiayu
AU - Duan, Hong
AU - Bejarano, Fernando
AU - Okamura, Katsutomo
AU - Fabian, Lacramioara
AU - Brill, Julie A.
AU - Bortolamiol-Becet, Diane
AU - Martin, Raquel
AU - Ruby, J. Graham
AU - Lai, Eric C.
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/1/8
Y1 - 2015/1/8
N2 - Although endogenous siRNAs (endo-siRNAs) have been described in many species, still little is known about their endogenous utility. Here, we show that Drosophila hairpin RNAs (hpRNAs) generate an endo-siRNA class with predominant expression in testes. Although hpRNAs are universally recently evolved, we identify highly complementary protein-coding targets for all hpRNAs. Importantly, we find broad evidence for evolutionary divergences that preferentially maintain compensatory pairing between hpRNAs and targets, serving as first evidence for adaptive selection for siRNA-mediated target regulation in metazoans. We demonstrate organismal impact of hpRNA activity, since knockout of hpRNA1 derepresses its target ATP synthase-β in testes and compromises spermatogenesis and male fertility. Moreover, we reveal surprising male-specific impact of RNAi factors on germ cell development and fertility, consistent with testis-directed function of the hpRNA pathway. Finally, the collected hpRNA loci chronicle an evolutionary timeline that reflects their origins from prospective target genes, mirroring a strategy described for plant miRNAs.
AB - Although endogenous siRNAs (endo-siRNAs) have been described in many species, still little is known about their endogenous utility. Here, we show that Drosophila hairpin RNAs (hpRNAs) generate an endo-siRNA class with predominant expression in testes. Although hpRNAs are universally recently evolved, we identify highly complementary protein-coding targets for all hpRNAs. Importantly, we find broad evidence for evolutionary divergences that preferentially maintain compensatory pairing between hpRNAs and targets, serving as first evidence for adaptive selection for siRNA-mediated target regulation in metazoans. We demonstrate organismal impact of hpRNA activity, since knockout of hpRNA1 derepresses its target ATP synthase-β in testes and compromises spermatogenesis and male fertility. Moreover, we reveal surprising male-specific impact of RNAi factors on germ cell development and fertility, consistent with testis-directed function of the hpRNA pathway. Finally, the collected hpRNA loci chronicle an evolutionary timeline that reflects their origins from prospective target genes, mirroring a strategy described for plant miRNAs.
UR - http://www.scopus.com/inward/record.url?scp=84920565409&partnerID=8YFLogxK
U2 - 10.1016/j.molcel.2014.11.025
DO - 10.1016/j.molcel.2014.11.025
M3 - Article
SN - 1097-2765
VL - 57
SP - 165
EP - 178
JO - Molecular Cell
JF - Molecular Cell
IS - 1
ER -