Marine Animal Disease Laboratory, School of Marine and Atmospheric Sciences, 100 Nicolls Road, Stony Brook University, Stony Brook, NY, 11794-5000, USA.
Sorbonne Université, CNRS, UMR 7144 AD2M, Station Biologique de Roscoff, Place Georges Teissier, 29688, Roscoff, France.
BMC Genomics. 2022 Mar 8;23(1):192. doi: 10.1186/s12864-021-08262-1.
The hard clam Mercenaria mercenaria is a major marine resource along the Atlantic coasts of North America and has been introduced to other continents for resource restoration or aquaculture activities. Significant mortality events have been reported in the species throughout its native range as a result of diseases (microbial infections, leukemia) and acute environmental stress. In this context, the characterization of the hard clam genome can provide highly needed resources to enable basic (e.g., oncogenesis and cancer transmission, adaptation biology) and applied (clam stock enhancement, genomic selection) sciences.
Using a combination of long and short-read sequencing technologies, a 1.86 Gb chromosome-level assembly of the clam genome was generated. The assembly was scaffolded into 19 chromosomes, with an N50 of 83 Mb. Genome annotation yielded 34,728 predicted protein-coding genes, markedly more than the few other members of the Venerida sequenced so far, with coding regions representing only 2% of the assembly. Indeed, more than half of the genome is composed of repeated elements, including transposable elements. Major chromosome rearrangements were detected between this assembly and another recent assembly derived from a genetically segregated clam stock. Comparative analysis of the clam genome allowed the identification of a marked diversification in immune-related proteins, particularly extensive tandem duplications and expansions in tumor necrosis factors (TNFs) and C1q domain-containing proteins, some of which were previously shown to play a role in clam interactions with infectious microbes. The study also generated a comparative repertoire highlighting the diversity and, in some instances, the specificity of LTR-retrotransposons elements, particularly Steamer elements in bivalves.
The diversity of immune molecules in M. mercenaria may allow this species to cope with varying and complex microbial and environmental landscapes. The repertoire of transposable elements identified in this study, particularly Steamer elements, should be a prime target for the investigation of cancer cell development and transmission among bivalve mollusks.
硬壳蛤 Mercenaria mercenaria 是北美的主要海洋资源之一,已被引入其他大洲用于资源恢复或水产养殖活动。由于疾病(微生物感染、白血病)和急性环境压力,该物种在其原生范围内已报告了重大死亡率事件。在这种情况下,硬壳蛤基因组的特征可以为基础科学(如致癌和癌症传播、适应生物学)和应用科学(蛤类资源增强、基因组选择)提供急需的资源。
使用长读长和短读长测序技术的组合,生成了蛤基因组的 1.86Gb 染色体水平组装。组装被支架到 19 条染色体中,N50 为 83Mb。基因组注释产生了 34728 个预测的蛋白质编码基因,明显多于迄今为止测序的其他几个 Venerida 成员,编码区仅占组装的 2%。事实上,基因组的一半以上由重复元件组成,包括转座元件。在这个组装和另一个来自遗传分离蛤种群的最近组装之间检测到主要的染色体重排。蛤基因组的比较分析允许鉴定出与免疫相关的蛋白质的显著多样化,特别是肿瘤坏死因子(TNFs)和 C1q 结构域蛋白的大量串联重复和扩展,其中一些先前被证明在蛤与传染性微生物相互作用中发挥作用。该研究还生成了一个比较库,突出了 LTR 反转录转座子元素的多样性,在某些情况下,还突出了其特异性,特别是双壳类动物中的 Steamer 元素。
M. mercenaria 中免疫分子的多样性可能使该物种能够应对不同和复杂的微生物和环境景观。本研究中鉴定的转座元件库,特别是 Steamer 元件,应该是调查双壳类软体动物中癌细胞发育和传播的主要目标。