Rapid Cis-Trans Coevolution Driven by a Novel Gene Retroposed from a Eukaryotic Conserved CCR4-NOT Component in Drosophila.
Rapid Cis-Trans Coevolution Driven by a Novel Gene Retroposed from a Eukaryotic Conserved CCR4-NOT Component in Drosophila.
复制标题
果蝇CCR 4-NOT真核保守区基因的快速顺反协同进化
DOI:
10.3390/genes13010057
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发表时间:
2021-12-26
期刊:
影响因子:
3.5
通讯作者:
Long M
中科院分区:
文献类型:
--
作者:
Krinsky BH;Arthur RK;Xia S;Sosa D;Arsala D;White KP;Long M
Young, or newly evolved, genes arise ubiquitously across the tree of life, and they can rapidly acquire novel functions that influence a diverse array of biological processes. Previous work identified a young regulatory duplicate gene in Drosophila, Zeus that unexpectedly diverged rapidly from its parent, Caf40, an extremely conserved component in the CCR4–NOT machinery in post-transcriptional and post-translational regulation of eukaryotic cells, and took on roles in the male reproductive system. This neofunctionalization was accompanied by differential binding of the Zeus protein to loci throughout the Drosophila melanogaster genome. However, the way in which new DNA-binding proteins acquire and coevolve with their targets in the genome is not understood. Here, by comparing Zeus ChIP-Seq data from D. melanogaster and D. simulans to the ancestral Caf40 binding events from D. yakuba, a species that diverged before the duplication event, we found a dynamic pattern in which Zeus binding rapidly coevolved with a previously unknown DNA motif, which we term Caf40 and Zeus-Associated Motif (CAZAM), under the influence of positive selection. Interestingly, while both copies of Zeus acquired targets at male-biased and testis-specific genes, D. melanogaster and D. simulans proteins have specialized binding on different chromosomes, a pattern echoed in the evolution of the associated motif. Using CRISPR-Cas9-mediated gene knockout of Zeus and RNA-Seq, we found that Zeus regulated the expression of 661 differentially expressed genes (DEGs). Our results suggest that the evolution of young regulatory genes can be coupled to substantial rewiring of the transcriptional networks into which they integrate, even over short evolutionary timescales. Our results thus uncover dynamic genome-wide evolutionary processes associated with new genes.
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DOI:
10.1093/bioinformatics/btr064
发表时间:
2011-04-01
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Grant CE;Bailey TL;Noble WS
通讯作者:
Noble WS
影响因子:
7
作者:
Arthur RK;Ma L;Slattery M;Spokony RF;Ostapenko A;Nègre N;White KP
通讯作者:
White KP
影响因子:
4.8
作者:
Bassett, Andrew;Liu, Ji-Long
通讯作者:
Liu, Ji-Long
DOI:
10.1073/pnas.0503528102
发表时间:
2005-08-09
影响因子:
11.1
作者:
Jones, CD;Begun, DJ
通讯作者:
Begun, DJ
影响因子:
5.6
作者:
Chen, JJ;Rappsilber, J;Denis, CL
通讯作者:
Denis, CL