Widespread Over-Expression of the X Chromosome in Sterile F1 Hybrid Mice

被引:93
作者
Good, Jeffrey M. [1 ,2 ,3 ]
Giger, Thomas [2 ]
Dean, Matthew D. [1 ,4 ]
Nachman, Michael W. [1 ]
机构
[1] Univ Arizona, Dept Ecol & Evolut Biol, Tucson, AZ 85721 USA
[2] Max Planck Inst Evolutionary Anthropol, Dept Evolutionary Genet, Leipzig, Germany
[3] Univ Montana, Div Biol Sci, Missoula, MT 59812 USA
[4] Univ So Calif, Los Angeles, CA USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
GENOME-WIDE PATTERNS; GENE-EXPRESSION; SEX-CHROMOSOMES; DROSOPHILA-SIMULANS; REPRODUCTIVE ISOLATION; UNISEXUAL STERILITY; MEIOTIC DRIVE; MOUSE; EVOLUTION; INACTIVATION;
D O I
10.1371/journal.pgen.1001148
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The X chromosome often plays a central role in hybrid male sterility between species, but it is unclear if this reflects underlying regulatory incompatibilities. Here we combine phenotypic data with genome-wide expression data to directly associate aberrant expression patterns with hybrid male sterility between two species of mice. We used a reciprocal cross in which F-1 males are sterile in one direction and fertile in the other direction, allowing us to associate expression differences with sterility rather than with other hybrid phenotypes. We found evidence of extensive over-expression of the X chromosome during spermatogenesis in sterile but not in fertile F-1 hybrid males. Over-expression was most pronounced in genes that are normally expressed after meiosis, consistent with an X chromosome-wide disruption of expression during the later stages of spermatogenesis. This pattern was not a simple consequence of faster evolutionary divergence on the X chromosome, because X-linked expression was highly conserved between the two species. Thus, transcriptional regulation of the X chromosome during spermatogenesis appears particularly sensitive to evolutionary divergence between species. Overall, these data provide evidence for an underlying regulatory basis to reproductive isolation in house mice and underscore the importance of transcriptional regulation of the X chromosome to the evolution of hybrid male sterility.
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页数:13
相关论文
共 85 条
[11]   Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data [J].
Dai, MH ;
Wang, PL ;
Boyd, AD ;
Kostov, G ;
Athey, B ;
Jones, EG ;
Bunney, WE ;
Myers, RM ;
Speed, TP ;
Akil, H ;
Watson, SJ ;
Meng, F .
NUCLEIC ACIDS RESEARCH, 2005, 33 (20) :e175.1-e175.9
[12]   Adaptive evolution of proteins secreted during sperm maturation: An analysis of the mouse epididymal transcriptome [J].
Dean, Matthem D. ;
Good, Jeffrey M. ;
Nachman, Michael W. .
MOLECULAR BIOLOGY AND EVOLUTION, 2008, 25 (02) :383-392
[13]   Proteomics and Comparative Genomic Investigations Reveal Heterogeneity in Evolutionary Rate of Male Reproductive Proteins in Mice (Mus domesticus) [J].
Dean, Matthew D. ;
Clark, Nathaniel L. ;
Findlay, Geoffrey D. ;
Karn, Robert C. ;
Yi, Xianhua ;
Swanson, Willie J. ;
MacCoss, Michael J. ;
Nachman, Michael W. .
MOLECULAR BIOLOGY AND EVOLUTION, 2009, 26 (08) :1733-1743
[14]   Enhanced Reprogramming of Xist by Induced Upregulation of Tsix and Dnmt3a [J].
Do, Jeong Tae ;
Han, Dong Wook ;
Gentile, Luca ;
Sobek-Klocke, Inge ;
Stehling, Martin ;
Schoeler, Hans R. .
STEM CELLS, 2008, 26 (11) :2821-2831
[15]   COUNTERSELECTION ON SEX-CHROMOSOMES IN THE MUS-MUSCULUS EUROPEAN HYBRID ZONE [J].
DOD, B ;
JERMIIN, LS ;
BOURSOT, P ;
CHAPMAN, VH ;
NIELSEN, JT ;
BONHOMME, F .
JOURNAL OF EVOLUTIONARY BIOLOGY, 1993, 6 (04) :529-546
[16]   Size, power and false discovery rates [J].
Efron, Bradley .
ANNALS OF STATISTICS, 2007, 35 (04) :1351-1377
[17]   GENETIC STUDIES ON MALE-STERILITY OF HYBRIDS BETWEEN LABORATORY AND WILD MICE (MUS-MUSCULUS L) [J].
FOREJT, J ;
IVANYI, P .
GENETICS RESEARCH, 1974, 24 (02) :189-+
[18]   MEIOTIC STUDIES OF TRANSLOCATIONS CAUSING MALE-STERILITY IN MOUSE .1. AUTOSOMAL RECIPROCAL TRANSLOCATIONS [J].
FOREJT, J ;
GREGOROVA, S .
CYTOGENETICS AND CELL GENETICS, 1977, 19 (2-3) :159-179
[19]  
FOREJT J, 1985, EXP CLIN IMMUNOGENET, V2, P106
[20]   Hybrid sterility in the mouse [J].
Forejt, J .
TRENDS IN GENETICS, 1996, 12 (10) :412-417