4.1 Article

Tracking Chromosomal Origins in the Northern Italy System of Metacentric Races of the House Mouse

期刊

CYTOGENETIC AND GENOME RESEARCH
卷 162, 期 4, 页码 214-229

出版社

KARGER
DOI: 10.1159/000527106

关键词

Robertsonian fusions; Whole-arm reciprocal translocations; Zonal raciation; Microsatellites; Mus musculus domesticus; Phylogenetics

资金

  1. Program Alssan (European Union Program of High Level Scholarships for Latin America) [E03D08916AR]
  2. Cornell Center for Vertebrate Genomics - CESAM - Centre for Environmental and Marine Studies through FCT/MCTES national funds [UIDP/50017/2020, UIDB/50017/2020, LA/P/0094/2020]
  3. Natural Environment Research Council, UK [Je-SRP1]
  4. European Union (Framework III HCM) [ERBCHRXCT930192]

向作者/读者索取更多资源

The Western European house mouse exhibits high chromosomal diversity, with various karyotypes resulting from Robertsonian fusion and reciprocal translocations. This study investigated the evolutionary relationships of chromosomal races within the Northern Italy System using centromere-adjacent microsatellite markers. The results suggested that these chromosomal races share a common origin and have likely undergone Robertsonian fusion and reciprocal translocations.
The Western European house mouse is chromosomally diverse, with diploid karyotypes ranging from the standard 40 telocentric chromosomes down to 22 chromosomes. Karyotypes are modified through Robertsonian (Rb) fusion of 2 telocentrics into a single metacentric, occurring repeatedly with fixation, and whole-arm reciprocal translocations (WARTs) generating additional novel karyotypes. Over 100 metacentric populations (chromosomal races) have been identified, geographically clustered into systems. Chromosomal races within systems often hybridise, and new races may emerge through this hybridisation (zonal raciation). We wished to determine the degree to which chromosomal races in a system have evolved independently or share common ancestry. Recombination between chromosomes from hybridising chromosomal races can erase the signals associated with a particular metacentric of interest, making inferences challenging. However, reduced recombination near the centromeres of chromosomal race-specific metacentrics makes centromere-adjacent markers ideal for solving this problem. For the Northern Italy System (NIS), we used microsatellite markers near the centromere to test previous hypotheses about evolutionary relationships of 5 chromosomal races. We chose markers from chromosomes 1, 3, 4, and 6, all of which comprise one arm of a metacentric in at least 2 of these NIS metacentric populations. We used estimates of F-ST and R-ST, as well as principal components analyses and neighbour-joining phylogenetic analyses, to infer evolutionary relationships between these 5 chromosomal races and neighbouring mice with the standard karyotype. We showed that the metacentric populations form a single grouping distinct from the standard populations, consistent with their common origin and consistent with a parsimonious sequence of chromosomal rearrangements to explain the relationship of the chromosomal races. That origin and evolution of the chromosomal races in the system would have involved Rb fusions, explaining the occurrence of chromosomal races with diploid numbers as low as 22. However, WARTs and zonal raciation have also been inferred, and the rare occurrence of chromosome 1 in different metacentrics in closely related chromosomal races is almost certainly explained by a WART. Our results with centromeric microsatellites are consistent with the above scenarios, illustrating, once again, the value of markers in the centromeric region to test evolutionary hypotheses in house mouse chromosomal systems.

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