The subgenomes show asymmetric expression of alleles in hybrid lineages of Megalobrama amblycephala × Culter alburnus
- Li Ren1,5,
- Wuhui Li1,5,
- Qinbo Qin1,5,
- He Dai2,5,
- Fengming Han2,
- Jun Xiao1,
- Xin Gao1,
- Jialin Cui1,
- Chang Wu1,
- Xiaojing Yan1,
- Guoliang Wang3,
- Guiming Liu3,
- Jia Liu1,
- Jiaming Li1,
- Zhong Wan4,
- Conghui Yang1,
- Chun Zhang1,
- Min Tao1,
- Jing Wang1,
- Kaikun Luo1,
- Shi Wang1,
- Fangzhou Hu1,
- Rurong Zhao1,
- Xuming Li2,
- Min Liu2,
- Hongkun Zheng2,
- Rong Zhou1,
- Yuqin Shu1,
- Yude Wang1,
- Qinfeng Liu1,
- Chenchen Tang1,
- Wei Duan1 and
- Shaojun Liu1
- 1State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Sciences, Hunan Normal University, Changsha 410081, China;
- 2Biomarker Technologies Corporation, Beijing 101300, China;
- 3Beijing Agro-Biotechnology Research Center, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China;
- 4School of Mathematics and Statistics, Central South University, Changsha 410083, China
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↵5 These authors contributed equally to this work.
Abstract
Hybridization drives rapid speciation by shaping novel genotypic and phenotypic profiles. Genomic incompatibility and transcriptome shock have been observed in hybrids, although this is rarer in animals than in plants. Using the newly sequenced genomes of the blunt snout bream (Megalobrama amblycephala [BSB]) and the topmouth culter (Culter alburnus [TC]), we focused on the sequence variation and gene expression changes in the reciprocal intergeneric hybrid lineages (F1–F3) of BSB × TC. A genome-wide transcriptional analysis identified 145–974 expressed recombinant genes in the successive generations of hybrid fish, suggesting the rapid emergence of allelic variation following hybridization. Some gradual changes of gene expression with additive and dominance effects and various cis and trans regulations were observed from F1 to F3 in the two hybrid lineages. These asymmetric patterns of gene expression represent the alternative strategies for counteracting deleterious effects of the subgenomes and improving adaptability of novel hybrids. Furthermore, we identified positive selection and additive expression patterns in transforming growth factor, beta 1b (tgfb1b), which may account for the morphological variations of the pharyngeal jaw in the two hybrid lineages. Our current findings provide insights into the evolution of vertebrate genomes immediately following hybridization.
Footnotes
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[Supplemental material is available for this article.]
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Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.249805.119.
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Freely available online through the Genome Research Open Access option.
- Received February 23, 2019.
- Accepted October 2, 2019.
This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.











