-
Something wrong with this record ?
Genome-wide architecture of reproductive isolation in a naturally occurring hybrid zone between Mus musculus musculus and M. m. domesticus
V. Janoušek, L. Wang, K. Luzynski, P. Dufková, MM. Vyskočilová, MW. Nachman, P. Munclinger, M. Macholán, J. Piálek, PK. Tucker,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.
- MeSH
- X Chromosome genetics MeSH
- Epistasis, Genetic MeSH
- Genetic Variation MeSH
- Hybridization, Genetic MeSH
- Polymorphism, Single Nucleotide MeSH
- Quantitative Trait Loci MeSH
- Mice genetics MeSH
- Reproductive Isolation MeSH
- Mating Preference, Animal MeSH
- Genetic Speciation MeSH
- Animals MeSH
- Check Tag
- Mice genetics MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
Studies of a hybrid zone between two house mouse subspecies (Mus musculus musculus and M. m. domesticus) along with studies using laboratory crosses reveal a large role for the X chromosome and multiple autosomal regions in reproductive isolation as a consequence of disrupted epistasis in hybrids. One limitation of previous work has been that most of the identified genomic regions have been large. The goal here is to detect and characterize precise genomic regions underlying reproductive isolation. We surveyed 1401 markers evenly spaced across the genome in 679 mice collected from two different transects. Comparisons between transects provide a means for identifying common patterns that likely reflect intrinsic incompatibilities. We used a genomic cline approach to identify patterns that correspond to epistasis. From both transects, we identified contiguous regions on the X chromosome in which markers were inferred to be involved in epistatic interactions. We then searched for autosomal regions showing the same patterns and found they constitute about 5% of autosomal markers. We discovered substantial overlap between these candidate regions underlying reproductive isolation and QTL for hybrid sterility identified in laboratory crosses. Analysis of gene content in these regions suggests a key role for several mechanisms, including the regulation of transcription, sexual conflict and sexual selection operating at both the postmating prezygotic and postzygotic stages of reproductive isolation. Taken together, these results indicate that speciation in two recently diverged (c. 0.5 Ma) house mouse subspecies is complex, involving many genes dispersed throughout the genome and associated with distinct functions.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13000810
- 003
- CZ-PrNML
- 005
- 20130110120612.0
- 007
- ta
- 008
- 130108s2012 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1111/j.1365-294x.2012.05583.x $2 doi
- 035 __
- $a (PubMed)22582810
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Janoušek, Václav $u Department of Zoology, Faculty of Science, Charles University in Prague, Viničná 7, 128 43 Prague 2, Czech Republic.
- 245 10
- $a Genome-wide architecture of reproductive isolation in a naturally occurring hybrid zone between Mus musculus musculus and M. m. domesticus / $c V. Janoušek, L. Wang, K. Luzynski, P. Dufková, MM. Vyskočilová, MW. Nachman, P. Munclinger, M. Macholán, J. Piálek, PK. Tucker,
- 520 9_
- $a Studies of a hybrid zone between two house mouse subspecies (Mus musculus musculus and M. m. domesticus) along with studies using laboratory crosses reveal a large role for the X chromosome and multiple autosomal regions in reproductive isolation as a consequence of disrupted epistasis in hybrids. One limitation of previous work has been that most of the identified genomic regions have been large. The goal here is to detect and characterize precise genomic regions underlying reproductive isolation. We surveyed 1401 markers evenly spaced across the genome in 679 mice collected from two different transects. Comparisons between transects provide a means for identifying common patterns that likely reflect intrinsic incompatibilities. We used a genomic cline approach to identify patterns that correspond to epistasis. From both transects, we identified contiguous regions on the X chromosome in which markers were inferred to be involved in epistatic interactions. We then searched for autosomal regions showing the same patterns and found they constitute about 5% of autosomal markers. We discovered substantial overlap between these candidate regions underlying reproductive isolation and QTL for hybrid sterility identified in laboratory crosses. Analysis of gene content in these regions suggests a key role for several mechanisms, including the regulation of transcription, sexual conflict and sexual selection operating at both the postmating prezygotic and postzygotic stages of reproductive isolation. Taken together, these results indicate that speciation in two recently diverged (c. 0.5 Ma) house mouse subspecies is complex, involving many genes dispersed throughout the genome and associated with distinct functions.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a genetická epistáze $7 D004843
- 650 _2
- $a vznik druhů (genetika) $7 D049810
- 650 _2
- $a genetická variace $7 D014644
- 650 _2
- $a hybridizace genetická $7 D006824
- 650 _2
- $a sexuální výběr u zvířat $7 D052586
- 650 _2
- $a myši $x genetika $7 D051379
- 650 _2
- $a jednonukleotidový polymorfismus $7 D020641
- 650 _2
- $a lokus kvantitativního znaku $7 D040641
- 650 _2
- $a reprodukční izolace $7 D060047
- 650 _2
- $a chromozom X $x genetika $7 D014960
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 655 _2
- $a Research Support, U.S. Gov't, Non-P.H.S. $7 D013486
- 700 1_
- $a Wang, Liuyang
- 700 1_
- $a Luzynski, Ken
- 700 1_
- $a Dufková, Petra
- 700 1_
- $a Vyskočilová, Martina M
- 700 1_
- $a Nachman, Michael W
- 700 1_
- $a Munclinger, Pavel
- 700 1_
- $a Macholán, Miloš
- 700 1_
- $a Piálek, Jaroslav
- 700 1_
- $a Tucker, Priscilla K
- 773 0_
- $w MED00006323 $t Molecular ecology $x 1365-294X $g Roč. 21, č. 12 (2012), s. 3032-47
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22582810 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20130108 $b ABA008
- 991 __
- $a 20130110120718 $b ABA008
- 999 __
- $a ok $b bmc $g 963592 $s 798974
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 21 $c 12 $d 3032-47 $i 1365-294X $m Molecular ecology $n Mol Ecol $x MED00006323
- LZP __
- $a Pubmed-20130108