低温深海南极秃艽--Trematomus borchgrevinki 的基因组。

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY G3: Genes|Genomes|Genetics Pub Date : 2024-11-16 DOI:10.1093/g3journal/jkae267
Niraj Rayamajhi, Angel G Rivera-Colón, Bushra Fazal Minhas, C-H Christina Cheng, Julian M Catchen
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引用次数: 0

摘要

南极秃艽(Trematomus borchgrevinki,艽科)生活在高纬度、多冰的环境中,是鱼类寒冷特化的一个极端例子。我们首次发现了一条雌性 T. borchgrevinki 的高质量染色体级基因组,该基因组由 23 条假定染色体组成,其中最大的一条染色体长达 65 兆位对 (Mbp)。基因组总长度为 935.13 Mbp,由 2,094 个支架组成,支架 N50 为 42.67 Mbp。通过注释获得了 22 192 个蛋白质编码基因,而基因组的 54.75% 被重复元素占据;重复分析表明,重复元素的扩大是在近期发生的。保守同源分析表明,博奇格雷文基蝾螈的基因组结构与notothenioid支系的其他成员基本保持一致,但存在几个重要的易位和倒位,包括将直向染色体8和11融合成一个元素。该基因组将作为冷特化模型,用于与notothenio适应性辐射的其他成员进行比较。
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The genome of the cryopelagic Antarctic bald notothen, Trematomus borchgrevinki.

The Antarctic bald notothen, Trematomus borchgrevinki (family Nototheniidae) occupies a high latitude, ice-laden environment and represents an extreme example of cold-specialization among fishes. We present the first, high quality, chromosome-scale genome of a female T. borchgrevinki individual comprised of 23 putative chromosomes, the largest of which is 65 megabasepairs (Mbp) in length. The total length of the genome 935.13 Mbp, composed of 2,094 scaffolds, with a scaffold N50 of 42.67 Mbp. Annotation yielded 22,192 protein coding genes while 54.75% of the genome was occupied by repetitive elements; an analysis of repeats demonstrated that an expansion occurred in recent time. Conserved synteny analysis revealed that the genome architecture of T. borchgrevinki is largely maintained with other members of the notothenioid clade, although several significant translocations and inversions are present, including the fusion of orthologous chromosomes 8 and 11 into a single element. This genome will serve as a cold-specialized model for comparisons to other members of the notothenioid adaptive radiation.

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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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