Neo-sex chromosomes in the black muntjac recapitulate incipient evolution of mammalian sex chromosomes.
Neo-sex chromosomes in the black muntjac recapitulate incipient evolution of mammalian sex chromosomes.
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黑麂的新性染色体再现了哺乳动物性染色体的早期进化。
DOI:
10.1186/gb-2008-9-6-r98
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发表时间:
2008
期刊:
影响因子:
12.3
通讯作者:
Wang W
中科院分区:
文献类型:
--
作者:
Zhou Q;Wang J;Huang L;Nie W;Wang J;Liu Y;Zhao X;Yang F;Wang W
The nascent neo-sex chromosomes of black muntjacs show that regulatory mutations could accelerate the degeneration of the Y chromosome and contribute to the further evolution of dosage compensation. The regular mammalian X and Y chromosomes diverged from each other at least 166 to 148 million years ago, leaving few traces of their early evolution, including degeneration of the Y chromosome and evolution of dosage compensation. We studied the intriguing case of black muntjac, in which a recent X-autosome fusion and a subsequent large autosomal inversion within just the past 0.5 million years have led to inheritance patterns identical to the traditional X-Y (neo-sex chromosomes). We compared patterns of genome evolution in 35-kilobase noncoding regions and 23 gene pairs on the homologous neo-sex chromosomes. We found that neo-Y alleles have accumulated more mutations, comprising a wide variety of mutation types, which indicates cessation of recombination and is consistent with an ongoing neo-Y degeneration process. Putative deleterious mutations were observed in coding regions of eight investigated genes as well as cis-regulatory regions of two housekeeping genes. In vivo assays characterized a neo-Y insertion in the promoter of the CLTC gene that causes a significant reduction in allelic expression. A neo-Y-linked deletion in the 3'-untranslated region of gene SNX22 abolished a microRNA target site. Finally, expression analyses revealed complex patterns of expression divergence between neo-Y and neo-X alleles. The nascent neo-sex chromosome system of black muntjacs is a valuable model in which to study the evolution of sex chromosomes in mammals. Our results illustrate the degeneration scenarios in various genomic regions. Of particular importance, we report - for the first time - that regulatory mutations were probably able to accelerate the degeneration process of Y and contribute to further evolution of dosage compensation.
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DOI:
10.1098/rstb.2000.0717
发表时间:
2000-11-29
影响因子:
6.3
作者:
Charlesworth, B;Charlesworth, D
通讯作者:
Charlesworth, D
影响因子:
--
作者:
Gupta V;Parisi M;Sturgill D;Nuttall R;Doctolero M;Dudko OK;Malley JD;Eastman PS;Oliver B
通讯作者:
Oliver B
影响因子:
9.2
作者:
Bachtrog, Doris
通讯作者:
Bachtrog, Doris
DOI:
10.1073/pnas.0504070102
发表时间:
2005-10-04
影响因子:
11.1
作者:
Drummond, DA;Bloom, JD;Arnold, FH
通讯作者:
Arnold, FH
影响因子:
3.9
作者:
Berlin, S;Brandström, M;Ellegren, H
通讯作者:
Ellegren, H