Evidence map›Paper›PMID 38177653›Full record

ArticleScientific reports2024

Chromosomal rearrangements played an important role in the speciation of rice rats of genus Cerradomys (Rodentia, Sigmodontinae, Oryzomyini).

Willam Oliveira da Silva, Stella Miranda Malcher, Malcolm Andrew Ferguson-Smith, Patricia Caroline Mary O'Brien, Rogério Vieira Rossi, Lena Geise, Julio Cesar Pieczarka, Cleusa Yoshiko Nagamachi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
11.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. The entireAntimicrobial agents and chemotherapy · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Chromoanagenesis and Beyond: Catastrophic Events Shaping the Genome.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Willam Oliveira da Silva *Laboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, Pará, Brazil.ORCID 0000-0003-3125-1075
Stella Miranda Malcher *Laboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, Pará, Brazil.
Malcolm Andrew Ferguson-SmithCambridge Resource Centre for Comparative Genomics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0001-9372-1381
Patricia Caroline Mary O'BrienCambridge Resource Centre for Comparative Genomics, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Rogério Vieira RossiDepartamento de Biologia e Zoologia, Instituto de Biociências, Universidade Federal do Mato Grosso (UFMT), Mato Grosso, Brazil.ORCID 0000-0003-2353-5000
Lena GeiseDepartamento de Zoologia, Laboratório de Mastozoologia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0003-1239-8047
Julio Cesar PieczarkaLaboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, Pará, Brazil.ORCID 0000-0003-2951-8877
Cleusa Yoshiko NagamachiLaboratório de Citogenética, Centro de Estudos Avançados da Biodiversidade, Instituto de Ciências Biológicas, Universidade Federal do Pará (UFPA), Belém, Pará, Brazil. cleusanagamachi@gmail.com.ORCID 0000-0003-1516-2734
Universidade Federal do Pará · BRUniversity of Cambridge · GBUniversidade do Estado do Rio de Janeiro · BRUniversidade Federal de Mato Grosso · BR

Funding

Banco Nacional de Desenvolvimento Econômico e Social - BNDES 2.318.697.0001Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 168394/2022-7Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 307154/2021-1Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 47290920096Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 552032/2010-7Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) 047/2012Fundação Amazônia Paraense de Amparo à Pesquisa (FAPESPA) 2010/110447Fundação Amazônia Paraense de Amparo à Pesquisa (FAPESPA) ICAAF 007/2011
6 · The paper itself

Abstract

Rodents of the genus Cerradomys belong to tribe Oryzomyini, one of the most diverse and speciose groups in Sigmodontinae (Rodentia, Cricetidae). The speciation process in Cerradomys is associated with chromosomal rearrangements and biogeographic dynamics in South America during the Pleistocene era. As the morphological, molecular and karyotypic aspects of Myomorpha rodents do not evolve at the same rate, we strategically employed karyotypic characters for the construction of chromosomal phylogeny to investigate whether phylogenetic relationships using chromosomal data corroborate the radiation of Cerradomys taxa recovered by molecular phylogeny. Comparative chromosome painting using Hylaeamys megacephalus (HME) whole chromosome probes in C. langguthi (CLA), Cerradomys scotii (CSC), C. subflavus (CSU) and C. vivoi (CVI) shows that karyotypic variability is due to 16 fusion events, 2 fission events, 10 pericentric inversions and 1 centromeric repositioning, plus amplification of constitutive heterochromatin in the short arms of the X chromosomes of CSC and CLA. The chromosomal phylogeny obtained by Maximum Parsimony analysis retrieved Cerradomys as a monophyletic group with 97% support (bootstrap), with CSC as the sister to the other species, followed by a ramification into two clades (69% of branch support), the first comprising CLA and the other branch including CVI and CSU. We integrated the chromosome painting analysis of Eumuroida rodents investigated by HME and Mus musculus (MMU) probes and identified several syntenic blocks shared among representatives of Cricetidae and Muridae. The Cerradomys genus underwent an extensive karyotypic evolutionary process, with multiple rearrangements that shaped extant karyotypes. The chromosomal phylogeny corroborates the phylogenetic relationships proposed by molecular analysis and indicates that karyotypic diversity is associated with species radiation. Three syntenic blocks were identified as part of the ancestral Eumuroida karyotype (AEK): MMU 7/19 (AEK 1), MMU 14 (AEK 10) and MMU 12 (AEK 11). Besides, MMU 5/10 (HME 18/2/24) and MMU 8/13 (HME 22/5/11) should be considered as signatures for Cricetidae, while MMU 5/9/14, 5/7/19, 5 and 8/17 for Sigmodontinae.

Indexed as

RodentiaSigmodontinaeAnimalsArvicolinaeChromosome InversionChromosome PaintingMuridaePhylogeny

Identifiers

PMID38177653
PMCPMC10766967
OpenAlexW4390579656

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.