Chromosomal and allozyme analysis of a hybrid zone between parapatric Robertsonian races of the house mouse: a case of monobrachial homology

2002 ◽  
Vol 96 (1-4) ◽  
pp. 75-84 ◽  
Author(s):  
J. Britton-Davidian ◽  
J. Catalan ◽  
K. Belkhir
Evolution ◽  
2012 ◽  
Vol 66 (9) ◽  
pp. 2757-2772 ◽  
Author(s):  
Stuart J. E. Baird ◽  
Alexis Ribas ◽  
Miloš Macholán ◽  
Tomáš Albrecht ◽  
Jaroslav Piálek ◽  
...  
Keyword(s):  

2016 ◽  
Vol 6 (9) ◽  
pp. 2688-2701 ◽  
Author(s):  
  Wasimuddin ◽  
Josef Bryja ◽  
Alexis Ribas ◽  
Stuart J. E. Baird ◽  
Jaroslav Piálek ◽  
...  
Keyword(s):  

Evolution ◽  
2011 ◽  
Vol 66 (2) ◽  
pp. 443-458 ◽  
Author(s):  
Leslie M. Turner ◽  
Denise J. Schwahn ◽  
Bettina Harr

Evolution ◽  
2011 ◽  
Vol 65 (4) ◽  
pp. 993-1010 ◽  
Author(s):  
Petra Dufková ◽  
Miloš Macholán ◽  
Jaroslav Piálek

2021 ◽  
Author(s):  
Alexey Yanchukov ◽  
Zusana Hiadlovska ◽  
Zeljka Pezer ◽  
Milos Macholan ◽  
Jaroslav Pialek ◽  
...  

Hybrid zones have long been described as "windows on the evolutionary process", and studying them has become even more important since the advance in the genome analysis tools. The hybrid zone between two subspecies of the house mouse (Mus musculus musculus and Mus m. domesticus) is a unique model speciation system to study fine scale interactions of recently diverged genomes. Here, we explore the role of gene Copy Number Variation in shaping the barrier to introgression in the hybrid zone within a previously established transect in Central Europe. The CNV of seven pre-selected candidate genes was determined via droplet-digital PCR and analyzed in the context of ~500k SNPs, with the ancestral population (i.e. musculus or domesticus) of every SNP allele previously inferred in the admixed individuals (Baird et al., in prep.). The copy numbers of five genes were clearly associated with the prevalence of either musculus or domesticus genomes across the hybrid zone. In three cases, the highest and/or outlying levels of association were observed at or very close to the annotated positions of the respective gene amplicons, demonstrating the power of our approach in confirming the reference locations of copy number variants. Notably, several other reference locations were recognized as positive outliers in the association with particular CNV genes, possibly representing the extra gene copies and/or their epistatic interaction sites.


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