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环口螈属(Cycloramphus)(无尾目,Cycloramphidae)染色体进化的更多线索:波纹唇鱼(Werner,1897)的细胞遗传学特征和重复 DNA 的定位

Cytogenetic characterization and mapping of the repetitive DNAs in Cycloramphus bolitoglossus (Werner, 1897): More clues for the chromosome evolution in the genus Cycloramphus (Anura, Cycloramphidae).

机构信息

Departamento de Genética, Setor de Ciências Biológicas, Universidade Federal do Paraná (UFPR), Curitiba, Paraná, Brazil.

Departamento de Biodiversidade e Centro de Aquicultura, Instituto de Biociências, Universidade Estadual Paulista, (UNESP), Rio Claro, São Paulo, Brazil.

出版信息

PLoS One. 2021 Jan 13;16(1):e0245128. doi: 10.1371/journal.pone.0245128. eCollection 2021.

DOI:10.1371/journal.pone.0245128
PMID:33439901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7806164/
Abstract

Cycloramphus bolitoglossus (Werner, 1897) is a rare species with a low population density in the Serra do Mar region of Paraná and Santa Catarina, in southern Brazil. Currently, it has been assigned to the Near Threatened (NT) category in the Brazilian List of Endangered Animal Species. Here, we described the karyotype of this species for the first time and investigated the patterns of some repetitive DNA classes in the chromosomes using molecular cytogenetic approaches. We isolated, sequenced and mapped the 5S rDNA and the satellite DNA PcP190 of C. bolitoglossus, as well as mapped the telomeric sequences and seven microsatellites motifies [(GA)15, (CA)15, (GACA)4, (GATA)8, (CAG)10, (CGC)10, and (GAA)]10. Cycloramphus bolitoglossus has 2n = 26 chromosomes and a fundamental number (FN) equal to 52, with a highly conserved karyotype compared to other genus members. Comparative cytogenetic under the phylogenetic context of genus allowed evolutionary interpretations of the morphological changes in the homologs of pairs 1, 3, and 6 along with the evolutionary history of Cycloramphus. Two subtypes of 5S rDNA type II were isolated in C. bolitoglossus genome, and several comparative analysis suggests mixed effects of concerted and birth-and-death evolution acting in this repetitive DNA. The 5S rDNA II subtype "a" and "b" was mapped on chromosome 1. However, their different position along chromosome 1 provide an excellent chromosome marker for future studies. PcP190 satellite DNA, already reported for species of the families Hylidae, Hylodidae, Leptodactylidae, and Odontophrynidae, is scattered throughout the C. bolitoglossus genome, and even non-heterochromatic regions showed hybridization signals using the PcP190 probe. Molecular analysis suggests that PcP190 satellite DNA exhibit a high-level of homogenization of this sequence in the genome of C. bolitoglossus. The PcP190 satDNA from C. bolitoglossus represents a novel sequence group, compared to other anurans, based on its hypervariable region. Overall, the present data on repetitive DNA sequences showed pseudogenization evidence and corroborated the hypothesis of the emergence of satDNA from rDNA 5S clusters. These two arguments that reinforced the importance of the birth-and-death evolutionary model to explain 5S rDNA patterns found in anuran genomes.

摘要

环口蟾蜍(Cycloramphus bolitoglossus)是一种在巴西南部巴拉那州和圣卡塔琳娜州沿海山脉地区数量稀少、密度较低的稀有物种。目前,它在巴西濒危物种红色名录中被列为近危(NT)物种。在这里,我们首次描述了该物种的核型,并使用分子细胞遗传学方法研究了染色体中一些重复 DNA 类别的模式。我们分离、测序并绘制了环口蟾蜍的 5S rDNA 和卫星 DNA PcP190 的图谱,还绘制了端粒序列和 7 个微卫星-motifs [(GA)15、(CA)15、(GACA)4、(GATA)8、(CAG)10、(CGC)10 和 (GAA)]10。环口蟾蜍有 2n = 26 条染色体和一个基本数(FN)等于 52,与其他属成员相比,其核型高度保守。在属的系统发育背景下进行比较细胞遗传学研究,使我们能够对同源对 1、3 和 6 的形态变化以及环口蟾蜍的进化历史进行进化解释。在环口蟾蜍基因组中分离出两种类型的 5S rDNA Ⅱ型,并且多项比较分析表明,在这种重复 DNA 中,协同进化和起源与灭绝进化的混合作用。5S rDNA II 亚型“a”和“b”被定位在 1 号染色体上。然而,它们在 1 号染色体上的不同位置为未来的研究提供了一个极好的染色体标记。PcP190 卫星 DNA 已在 Hylidae、Hylodidae、Leptodactylidae 和 Odontophrynidae 科的物种中报道,它分散在环口蟾蜍的基因组中,甚至在非异染色质区域使用 PcP190 探针也显示出杂交信号。分子分析表明,PcP190 卫星 DNA 在环口蟾蜍的基因组中表现出该序列高度同源化。与其他两栖动物相比,来自环口蟾蜍的 PcP190 satDNA 在其高变区代表了一个新的序列群。总的来说,重复 DNA 序列的现有数据显示出假基因化的证据,并证实了 satDNA 从 rDNA 5S 簇出现的假说。这两个论点加强了起源与灭绝进化模型对解释在两栖动物基因组中发现的 5S rDNA 模式的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/4ba309c711be/pone.0245128.g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/51d60d5033b3/pone.0245128.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/4ba309c711be/pone.0245128.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/908e74e77cbc/pone.0245128.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/8f1556dad4a8/pone.0245128.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/477a66e25e53/pone.0245128.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/5ff211d5a30d/pone.0245128.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/51d60d5033b3/pone.0245128.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c6/7806164/4ba309c711be/pone.0245128.g006.jpg

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