帕拉斯猫的四个新的基因组序列(耳疣手册):对物种内变异模式的洞察。

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY
Frontiers in Genetics Pub Date : 2024-12-09 eCollection Date: 2024-01-01 DOI:10.3389/fgene.2024.1463774
Jana Bubenikova, Martin Plasil, Pamela A Burger, Petr Horin
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引用次数: 0

摘要

Manul(耳疣子)是耳疣子属的唯一代表,它与Prionailurus属一起构成了豹猫的血统。它们的栖息地环境条件恶劣。虽然它们的数量可能比以前认为的更稳定,但它们的数量仍然在下降。现有的保护计划是为了保护手工鱼,但那些基于圈养繁殖的计划往往不成功,因为它们对疾病的易感性增加。因此,该手册是进化和多样性研究以及研究对恶劣环境的适应机制和对疾病的易感性机制的合适模式物种。近年来,基于纳米孔远程测序的欧曼氏菌基因组已被报道。为了更好地了解该物种的种间和种内变异,我们基于Illumina平台的全基因组重测序,获得了其他四个物种的基因组序列信息。平均而言,我们共检测到3,636,571个多态性变异。检索了不同类型的结构变异和SNP纯合程度的信息,这些信息无法从参考基因组中获得。平均全基因组杂合性与O. manual参考基因组几乎相同。在此背景下,我们对候选基因EPAS1进行了更详细的分析,该基因可能与适应低氧环境有关。该分析揭示了种间和种内变异,证实了先前描述的manual特有的第15外显子非同义替换的存在,并确定了位于迄今未分析的EPAS1外显子序列中的另外三个独特的非同义替换。对位于EPAS1内含子7上的lncRNA的分析揭示了该序列在被分析的基因组中的种间变异性和单态性。获得的数据将允许对人工基因组进行更详细的分析,重点关注与它们适应环境和对疾病易感性有关的基因和途径。这些信息有助于优化这一未被充分研究的物种的保护计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Four new genome sequences of the Pallas's cat (Otocolobus manul): an insight into the patterns of within-species variability.

Manul (Otocolobus manul) is the only representative of the genus Otocolobus, which makes up the Leopard Cat lineage along with the genus Prionailurus. Their habitat is characterized by harsh environmental conditions. Although their populations are probably more stable than previously thought, it is still the case that their population size is declining. Conservation programs exist to protect manuls, but those based on captive breeding are often unsuccessful due to their increased susceptibility to diseases. The manul is therefore a suitable model species for evolutionary and diversity studies as well as for studying mechanisms of adaptation to harsh environment and mechanisms of susceptibility to diseases. Recently, the genome of the O. manul based on nanopore long-range sequencing has been published. Aiming to better understand inter- and intraspecific variation of the species, we obtained information on genome sequences of four other manuls, based on whole genome resequencing via the Illumina platform. On average, we detected a total of 3,636,571 polymorphic variants. Information on different types of structural variants and on the extent of SNP homozygosity, not available from the reference genome, was retrieved. The average whole-genome heterozygosity was almost identical to that found in the O. manul reference genome. In this context, we performed a more detailed analysis of the candidate gene EPAS1 potentially related to adaptation to the hypoxic environment. This analysis revealed both inter- and intraspecific variation, confirmed the presence of a previously described non-synonymous substitution in exon 15 unique to manuls and identified three additional unique non-synonymous substitutions located in so far not analyzed EPAS1 exonic sequences. The analysis of lncRNA located in the intron 7 of EPAS1 revealed interspecific variability and monomorphic nature of the sequence among analyzed manuls. The data obtained will allow more detailed analyses of the manul genome, focusing on genes and pathways involved in their adaptation to the environment and in susceptibility to diseases. This information can be helpful for optimizing conservation programs for this understudied species.

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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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