cis-by-trans regulatory divergence causes the asymmetric lethal effects of an ancestral hybrid incompatibility genecis-by-trans监管差异造成的不对称的致命影响一个祖先的基因混合不相容.pdfVIP

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cis-by-trans regulatory divergence causes the asymmetric lethal effects of an ancestral hybrid incompatibility genecis-by-trans监管差异造成的不对称的致命影响一个祖先的基因混合不相容.pdf

cis-by-trans regulatory divergence causes the asymmetric lethal effects of an ancestral hybrid incompatibility genecis-by-trans监管差异造成的不对称的致命影响一个祖先的基因混合不相容

Cis-by-Trans Regulatory Divergence Causes the Asymmetric Lethal Effects of an Ancestral Hybrid Incompatibility Gene Shamoni Maheshwari, Daniel A. Barbash* Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America Abstract The Dobzhansky and Muller (D-M) model explains the evolution of hybrid incompatibility (HI) through the interaction between lineage-specific derived alleles at two or more loci. In agreement with the expectation that HI results from functional divergence, many protein-coding genes that contribute to incompatibilities between species show signatures of adaptive evolution, including Lhr, which encodes a heterochromatin protein whose amino acid sequence has diverged extensively between Drosophila melanogaster and D. simulans by natural selection. The lethality of D. melanogaster/D. simulans F1 hybrid sons is rescued by removing D. simulans Lhr, but not D. melanogaster Lhr, suggesting that the lethal effect results from adaptive evolution in the D. simulans lineage. It has been proposed that adaptive protein divergence in Lhr reflects antagonistic coevolution with species-specific heterochromatin sequences and that defects in LHR protein localization cause hybrid lethality. Here we present surprising results that are inconsistent with this coding-sequence-based model. Using Lhr transgenes expressed under native conditions, we find no evidence that LHR localization differs between D. melanogaster and D. simulans, nor do we find evidence that it mislocalizes in their interspecific hybrids. Rather, we demonstrate that Lhr orthologs are differentially expressed in the hybrid background, with the levels of D. simulans Lhr double that of D. melanogaster Lhr. We further show that this asymmetric expression is caused by

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