Mitochondrial genome of a Bolivian River Dolphin (Inia boliviensis).

IF 0.7 4区 生物学 Q4 GENETICS & HEREDITY
Mitochondrial DNA. Part B, Resources Pub Date : 2025-08-11 eCollection Date: 2025-01-01 DOI:10.1080/23802359.2025.2544682
Kristin Coury, Ellen Bronson, Claudia Venegas Cuzmar, Sharon Deem, Jacqueline M Doyle
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引用次数: 0

Abstract

Inia boliviensis, the endemic Bolivian river dolphin, is threatened by anthropogenic activities including diversion of waterways for irrigation of agricultural fields, habitat degradation through deforestation, and the construction of hydroelectric dams. Within the department of Santa Cruz in Bolivia, conservation partners are committed to the capture and relocation of river dolphins that have been isolated through seasonally changing waterways, which are exacerbated by anthropogenic changes to local rivers' courses. During these rescue attempts, tissue samples were taken to better understand the genetic composition of the fragmented populations. Herein, we describe the newly sequenced and assembled Bolivian river dolphin mitochondrial genome. The genome assembly is 16,591 base pairs in length, with an overall base composition of 32.75% adenine, 25.85% thymine, 28.35% cytosine, and 13.05% guanine. This resource will pave the way for a better understanding of Bolivian river dolphin population genetics, which will help inform effective management of these vulnerable populations.

玻利维亚河豚(Inia boliviensis)线粒体基因组。
玻利维亚特有的河豚Inia boliviensis正受到人为活动的威胁,这些活动包括为农田灌溉而改道、森林砍伐导致栖息地退化以及建设水电站大坝。在玻利维亚的圣克鲁斯省,保护伙伴们致力于捕捉和重新安置那些因季节性变化的水道而孤立的河豚,这些河流因当地河流的人为变化而加剧。在这些救援尝试中,采集了组织样本,以更好地了解碎片化种群的遗传组成。在这里,我们描述了新测序和组装玻利维亚河豚线粒体基因组。基因组全长16591个碱基对,总碱基组成为32.75%的腺嘌呤、25.85%的胸腺嘧啶、28.35%的胞嘧啶和13.05%的鸟嘌呤。这一资源将为更好地了解玻利维亚河豚种群遗传学铺平道路,这将有助于对这些脆弱种群进行有效管理。
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来源期刊
Mitochondrial DNA. Part B, Resources
Mitochondrial DNA. Part B, Resources Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
1.30
自引率
20.00%
发文量
670
期刊介绍: This open access journal publishes high-quality and concise research articles reporting the sequence of full mitochondrial genomes, and short communications focusing on the physical, chemical, and biochemical aspects of mtDNA and proteins involved in mtDNA metabolism and interactions.
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