De novo genome assembly and annotations of Bombus lapidarius and Bombus niveatus provide insights into the environmental adaptability

IF 2.4 3区 农林科学 Q1 ENTOMOLOGY
Vahap Eldem, Yusuf Ulaş Çınar, Selahattin Barış Çay, Onur Obut, Selim Can Kuralay, Mehmet Ali Balcı, Pınar Akbaba, Tuana Öğretici, Tunç Dabak, Burcu Daşer Özgişi, Çiğdem Özenirler, Gökmen Zararsız, Esma Gamze Aksel, Fatih Dikmen
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引用次数: 0

Abstract

Bumblebees are ubiquitous, cold-adapted, primitively eusocial bees and important pollinators for crops and vegetation. However, many species are declining worldwide due to multiple factors, including human-induced habitat loss, agricultural chemicals, global warming, and climate change. In particular, future climate scenarios predict a shift in the spatial distribution of bumblebees under global warming, with some species declining and others potentially expanding. Here, we report a de novo genome assembly and annotation for Bombus lapidarius and Bombus niveatus to decipher species-specific potential genomic capacity against such environmental stressors. With harboring more than 23,000 protein-coding genes, the assembled genomes of B. lapidarius and B. niveatus are 244.44 Mb (scaffold N50 of 9.45 Mb) and 259.84 Mb (scaffold N50 of 10.94 Mb), respectively, which exhibit similar trends in terms of genome size and composition with other bumblebees. Gene family analysis reveals differences in species-specific expanded gene families. B. lapidarius exhibits expanded genes related to pre/postsynaptic organization, while B. niveatus shows a distinct expansion in gene families regulating cellular growth, aging, and responses to abiotic and biotic stressors, such as those containing SCAN domains, WD-repeats, and Ras-related proteins. Our genome-wide screens revealed positive selection on environmental stress-responsive genes such as dip2, yme1l, and spg7 in B. lapidarius, whereas positive selection signatures were found in genes such as myd88, mybbp1A, and rhau, which are involved in environmental stress resistance for B. niveatus. These high-quality genome assemblies and comparative genome analysis unveil potential drivers that underlie genome evolution in bumblebees, offering valuable insights into environmental adaptation and conservation efforts.

石菖蒲和牛菖蒲的从头基因组组装和注释为研究其环境适应性提供了新的思路
大黄蜂是普遍存在的,适应寒冷的原始群居蜜蜂,也是农作物和植被的重要传粉者。然而,由于人类活动导致的栖息地丧失、农业化学品、全球变暖和气候变化等多种因素,世界范围内许多物种正在减少。特别是,未来的气候情景预测,在全球变暖的情况下,大黄蜂的空间分布将发生变化,一些物种将减少,另一些物种可能会扩大。在这里,我们报道了一种全新的基因组组装和注释,以破译物种特异性的针对这些环境胁迫的潜在基因组能力。石蜡小蜂和牛头小蜂组装的基因组分别为244.44 Mb(支架N50为9.45 Mb)和259.84 Mb(支架N50为10.94 Mb),包含23000多个蛋白质编码基因,在基因组大小和组成上与其他大黄蜂相似。基因家族分析揭示了物种特异性扩展基因家族的差异。石斑鱼显示出与突触前/突触后组织相关的基因扩展,而牛牙鱼在调节细胞生长、衰老和对非生物和生物应激源的反应的基因家族中显示出明显的扩展,例如那些含有SCAN结构域、wd重复序列和ras相关蛋白的基因家族。我们的全基因组筛选结果显示,石斑白螺旋藻中dip2、yme1l和sp7等环境应激响应基因存在正选择,而niveatus中myd88、mybbp1A和rhau等基因则存在正选择特征,这些基因与环境应激抗性有关。这些高质量的基因组组装和比较基因组分析揭示了大黄蜂基因组进化的潜在驱动因素,为环境适应和保护工作提供了有价值的见解。
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来源期刊
Apidologie
Apidologie 生物-昆虫学
CiteScore
5.10
自引率
8.30%
发文量
64
审稿时长
3 months
期刊介绍: Apidologie is a peer-reviewed journal devoted to the biology of insects belonging to the superfamily Apoidea. Its range of coverage includes behavior, ecology, pollination, genetics, physiology, systematics, toxicology and pathology. Also accepted are papers on the rearing, exploitation and practical use of Apoidea and their products, as far as they make a clear contribution to the understanding of bee biology. Apidologie is an official publication of the Institut National de la Recherche Agronomique (INRA) and Deutscher Imkerbund E.V. (D.I.B.)
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