冰川融化前小尺度生境异质性和基因型调节南极双壳类动物原位基因表达。

IF 2.3 Q2 ECOLOGY
Mariano Martínez, Lars Harms, Doris Abele, Christoph Held
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引用次数: 0

摘要

基因表达调控是生物面对环境变化的关键适应机制。在南极洲乔治王岛波特湾(Potter Cove),研究了在融化冰川前不同栖息地的浅水双壳类动物Aequiyoldia eightsii的原位基因表达。核基因的表达取决于(1)核基因组本身的变异(核snp),同样重要的是取决于(2)三个位置的不同环境条件和(3)线粒体基因型的组成(线粒体snp)。线粒体snp将南极动物分为两组,每组由线粒体同源性和异质性的生物组成。我们通过将观察到的差异表达基因(deg)的大小与随机分组比较中随机性预期的大小进行比较,验证了我们的结果。生境比较进一步揭示了局部尺度上deg的差异,表明对特定微环境具有较高的进化适应潜力。有趣的是,有丝分裂型之间的差异表达分析导致的deg数量比通过站比较获得的要高,从而区分了异质和同质生物体。我们的研究结果表明,线粒体基因组和可能的异质性可能在核基因表达调控中发挥作用,具有适应性意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Small-scale habitat heterogeneity and genotype modulate in situ gene expression of the Antarctic bivalve Aequiyoldia eightsii in front of a melting glacier.

Regulation of gene expression is a pivotal adaptive mechanism of organisms facing environmental variation. We studied the in situ gene expression of the shallow-water bivalve Aequiyoldia eightsii in Potter Cove (King George Island, Antarctica) occupying different habitats in front of a melting glacier on a local scale (1 km). The expression of nuclear genes was determined by (1) variation of the nuclear genome itself (nuclear SNPs) and equally strongly by (2) different environmental conditions characterizing the three locations and (3) the composition of the mitochondrial genotype (mitochondrial SNPs). Mitochondrial SNPs divided Antarctic animals into two groups, each composed of organisms featuring mitochondrial homoplasmy and heteroplasmy. We validated our results by contrasting the observed magnitudes of differentially expressed genes (DEGs) with magnitudes expected by stochasticity in randomized group comparisons. Habitat comparison revealed further differences in DEGs at local scale suggesting a high evolutionary adaptive potential to the specific microenvironments. Interestingly, differential expression analysis between mitotypes resulted in a higher number of DEGs than the obtained in the comparison by stations, distinguishing heteroplasmic from homoplasmic organisms. Our results suggest that the mitochondrial genome and possibly heteroplasmy may play a role in the regulation of nuclear gene expression with adaptive implications.

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