Laboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, Pará, Brazil.
Instituto de Biologia Subtropical (CONICET-UNAM), Puerto Iguazú, Misiones, Argentina.
PLoS One. 2021 Oct 11;16(10):e0258474. doi: 10.1371/journal.pone.0258474. eCollection 2021.
Rhipidomys (Sigmodontinae, Thomasomyini) has 25 recognized species, with a wide distribution ranging from eastern Panama to northern Argentina. Cytogenetic data has been described for 13 species with 12 of them having 2n = 44 with a high level of autosomal fundamental number (FN) variation, ranging from 46 to 80, assigned to pericentric inversions. The species are grouped in groups with low FN (46-52) and high FN (72-80). In this work the karyotypes of Rhipidomys emiliae (2n = 44, FN = 50) and Rhipidomys mastacalis (2n = 44, FN = 74), were studied by classical cytogenetics and by fluorescence in situ hybridization using telomeric and whole chromosome probes (chromosome painting) of Hylaeamys megacephalus (HME). Chromosome painting revealed homology between 36 segments of REM and 37 of RMA. We tested the hypothesis that pericentric inversions are the predominant chromosomal rearrangements responsible for karyotypic divergence between these species, as proposed in literature. Our results show that the genomic diversification between the karyotypes of the two species resulted from translocations, centromeric repositioning and pericentric inversions. The chromosomal evolution in Rhipidomys was associated with karyotypical orthoselection. The HME probes revealed that seven syntenic probably ancestral blocks for Sigmodontinae are present in Rhipidomys. An additional syntenic block described here is suggested as part of the subfamily ancestral karyotype. We also define five synapomorphies that can be used as chromosomal signatures for Rhipidomys.
(刺毛鼠亚科、托马斯鼠亚科)有 25 个公认的物种,分布范围从巴拿马东部到阿根廷北部。已经描述了 13 个物种的细胞遗传学数据,其中 12 个物种的 2n = 44,具有高水平的常染色体基数(FN)变异,范围从 46 到 80,归因于着丝粒倒位。这些物种分为 FN 较低(46-52)和 FN 较高(72-80)的组。在这项工作中,通过经典细胞遗传学和荧光原位杂交(使用 Hylaeamys megacephalus(HME)的端粒和整条染色体探针(染色体标记))研究了 Rhipidomys emiliae(2n = 44,FN = 50)和 Rhipidomys mastacalis(2n = 44,FN = 74)的核型。染色体标记揭示了 REM 的 36 个片段和 RMA 的 37 个片段之间的同源性。我们测试了这样一个假设,即着丝粒倒位是导致这些物种之间核型分化的主要染色体重排,正如文献中所提出的那样。我们的结果表明,这两个物种的核型之间的基因组多样化是由易位、着丝粒重定位和着丝粒倒位引起的。刺毛鼠的染色体进化与核型同形选择有关。HME 探针表明,Sigmodontinae 有七个可能的祖先同源块存在于 Rhipidomys 中。这里描述的另一个同源块被认为是亚科祖先核型的一部分。我们还定义了五个可以作为刺毛鼠染色体特征的共衍特征。