Khudyakov Jane I, Preeyanon Likit, Champagne Cory D, Ortiz Rudy M, Crocker Daniel E
Department of Biology, Sonoma State University, 1801 E Cotati Ave, Rohnert Park, CA, 94928, USA.
Michigan State University, Microbiology and Molecular Genetics, 567 Wilson Rd, East Lansing, MI, 48824, USA.
BMC Genomics. 2015 Feb 8;16(1):64. doi: 10.1186/s12864-015-1253-6.
The northern elephant seal, Mirounga angustirostris, is a valuable animal model of fasting adaptation and hypoxic stress tolerance. However, no reference sequence is currently available for this and many other marine mammal study systems, hindering molecular understanding of marine adaptations and unique physiology.
We sequenced a transcriptome of M. angustirostris derived from muscle sampled during an acute stress challenge experiment to identify species-specific markers of stress axis activation and recovery. De novo assembly generated 164,966 contigs and a total of 522,699 transcripts, of which 68.70% were annotated using mouse, human, and domestic dog reference protein sequences. To reduce transcript redundancy, we removed highly similar isoforms in large gene families and produced a filtered assembly containing 336,657 transcripts. We found that a large number of annotated genes are associated with metabolic signaling, immune and stress responses, and muscle function. Preliminary differential expression analysis suggests a limited transcriptional response to acute stress involving alterations in metabolic and immune pathways and muscle tissue maintenance, potentially driven by early response transcription factors such as Cebpd.
We present the first reference sequence for Mirounga angustirostris produced by RNA sequencing of muscle tissue and cloud-based de novo transcriptome assembly. We annotated 395,102 transcripts, some of which may be novel isoforms, and have identified thousands of genes involved in key physiological processes. This resource provides elephant seal-specific gene sequences, complementing existing metabolite and protein expression studies and enabling future work on molecular pathways regulating adaptations such as fasting, hypoxia, and environmental stress responses in marine mammals.
北象海豹(Mirounga angustirostris)是禁食适应和低氧应激耐受的重要动物模型。然而,目前该物种以及许多其他海洋哺乳动物研究系统都没有参考序列,这阻碍了对海洋适应性和独特生理学的分子理解。
我们对在急性应激挑战实验中采集的北象海豹肌肉转录组进行了测序,以确定应激轴激活和恢复的物种特异性标记。从头组装产生了164,966个重叠群和总共522,699个转录本,其中68.70% 使用小鼠、人类和家犬参考蛋白质序列进行了注释。为了减少转录本冗余,我们去除了大基因家族中高度相似的异构体,并生成了一个包含336,657个转录本的过滤组装。我们发现大量注释基因与代谢信号传导、免疫和应激反应以及肌肉功能相关。初步差异表达分析表明,对急性应激的转录反应有限,涉及代谢和免疫途径以及肌肉组织维持的改变,可能由早期反应转录因子如Cebpd驱动。
我们展示了通过肌肉组织RNA测序和基于云的从头转录组组装产生的北象海豹首个参考序列。我们注释了395,102个转录本,其中一些可能是新的异构体,并确定了数千个参与关键生理过程的基因。该资源提供了象海豹特异性基因序列,补充了现有的代谢物和蛋白质表达研究,并为未来研究调节海洋哺乳动物禁食、低氧和环境应激反应等适应性的分子途径提供了可能。