Extensive Chromosomal Reorganization in the Evolution of New World Muroid Rodents (Cricetidae, Sigmodontinae): Searching for Ancestral Phylogenetic Traits

PLoS One. 2016 Jan 22;11(1):e0146179. doi: 10.1371/journal.pone.0146179. eCollection 2016.

Abstract

Sigmodontinae rodents show great diversity and complexity in morphology and ecology. This diversity is accompanied by extensive chromosome variation challenging attempts to reconstruct their ancestral genome. The species Hylaeamys megacephalus--HME (Oryzomyini, 2n = 54), Necromys lasiurus--NLA (Akodontini, 2n = 34) and Akodon sp.--ASP (Akodontini, 2n = 10) have extreme diploid numbers that make it difficult to understand the rearrangements that are responsible for such differences. In this study we analyzed these changes using whole chromosome probes of HME in cross-species painting of NLA and ASP to construct chromosome homology maps that reveal the rearrangements between species. We include data from the literature for other Sigmodontinae previously studied with probes from HME and Mus musculus (MMU) probes. We also use the HME probes on MMU chromosomes for the comparative analysis of NLA with other species already mapped by MMU probes. Our results show that NLA and ASP have highly rearranged karyotypes when compared to HME. Eleven HME syntenic blocks are shared among the species studied here. Four syntenies may be ancestral to Akodontini (HME2/18, 3/25, 18/25 and 4/11/16) and eight to Sigmodontinae (HME26, 1/12, 6/21, 7/9, 5/17, 11/16, 20/13 and 19/14/19). Using MMU data we identified six associations shared among rodents from seven subfamilies, where MMU3/18 and MMU8/13 are phylogenetic signatures of Sigmodontinae. We suggest that the associations MMU2entire, MMU6proximal/12entire, MMU3/18, MMU8/13, MMU1/17, MMU10/17, MMU12/17, MMU5/16, MMU5/6 and MMU7/19 are part of the ancestral Sigmodontinae genome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Evolution
  • Chromosome Banding
  • Chromosome Painting
  • Chromosomes*
  • Female
  • Heterochromatin / genetics
  • In Situ Hybridization, Fluorescence
  • Karyotype
  • Male
  • Phylogeny*
  • Sigmodontinae / genetics*

Substances

  • Heterochromatin

Grants and funding

This work was supported by Proc 552032/2010-7, Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (http://www.cnpq.br; ICAAF 007/2011); Fundação de Amparo à Pesquisa do Estado do Pará (FAPESPA) (http://www.fapespa.pa.gov.br); Proc 2010/110447, Fundação de Amparo à Pesquisa do Estado do Pará (FAPESPA) (http://www.fapespa.pa.gov.br). S. M. Malcher is the recipient of a CAPES Doctor Scholarship in Neuroscience and Cell Biology, and A. L. Pereira is the recipient of a CAPES Doctor Scholarship in Genetics and Molecular Biology. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.