一种用于研究秀丽隐杆线虫核体肌肉形成和功能的最新转录组。

IF 5.3 2区 医学 Q2 CELL BIOLOGY Skeletal Muscle Pub Date : 2023-03-02 DOI:10.1186/s13395-023-00314-2
Anna L Schorr, Alejandro Felix Mejia, Martina Y Miranda, Marco Mangone
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引用次数: 1

摘要

身体肌肉是机体维持正常生存和运动的重要组织。尽管这种组织通常被很好地研究和表征,并且多年来已经阐明了许多途径,但我们仍然缺乏对其转录组及其如何控制肌肉发育和功能的全面了解。在这里,我们更新了一种基于核FACS分选的方法,从秀丽隐杆线虫混合期动物中分离和测序高质量的肌肉转录组。我们已经确定了2848个肌肉特异性蛋白质编码基因,包括78个转录因子和206个含有RNA结合域的蛋白质编码基因。我们研究了它们的相互作用网络,进行了详细的启动子分析,并确定了新的肌肉特异性顺式作用元件。我们还鉴定了16个高质量的肌肉特异性miRNA,使用基于荧光色的分析研究了它们在体内的功能,并开发了一个高质量的秀丽隐杆线虫miRNA相互作用组,其中包含了我们实验室和其他实验室生产的其他肌肉特异性数据集。我们的研究扩展了我们对秀丽隐杆线虫肌肉组织功能的理解,反过来提供了可以在未来应用于人类研究肌肉相关疾病的结果。
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An updated C. elegans nuclear body muscle transcriptome for studies in muscle formation and function.

The body muscle is an important tissue used in organisms for proper viability and locomotion. Although this tissue is generally well studied and characterized, and many pathways have been elucidated throughout the years, we still lack a comprehensive understanding of its transcriptome and how it controls muscle development and function. Here, we have updated a nuclear FACS sorting-based methodology to isolate and sequence a high-quality muscle transcriptome from Caenorhabditis elegans mixed-stage animals. We have identified 2848 muscle-specific protein-coding genes, including 78 transcription factors and 206 protein-coding genes containing an RNA binding domain. We studied their interaction network, performed a detailed promoter analysis, and identified novel muscle-specific cis-acting elements. We have also identified 16 high-quality muscle-specific miRNAs, studied their function in vivo using fluorochrome-based analyses, and developed a high-quality C. elegans miRNA interactome incorporating other muscle-specific datasets produced by our lab and others.Our study expands our understanding of how muscle tissue functions in C. elegans andin turn provides results that can in the future be applied to humans to study muscular-related diseases.

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来源期刊
Skeletal Muscle
Skeletal Muscle CELL BIOLOGY-
CiteScore
9.10
自引率
0.00%
发文量
25
审稿时长
12 weeks
期刊介绍: The only open access journal in its field, Skeletal Muscle publishes novel, cutting-edge research and technological advancements that investigate the molecular mechanisms underlying the biology of skeletal muscle. Reflecting the breadth of research in this area, the journal welcomes manuscripts about the development, metabolism, the regulation of mass and function, aging, degeneration, dystrophy and regeneration of skeletal muscle, with an emphasis on understanding adult skeletal muscle, its maintenance, and its interactions with non-muscle cell types and regulatory modulators. Main areas of interest include: -differentiation of skeletal muscle- atrophy and hypertrophy of skeletal muscle- aging of skeletal muscle- regeneration and degeneration of skeletal muscle- biology of satellite and satellite-like cells- dystrophic degeneration of skeletal muscle- energy and glucose homeostasis in skeletal muscle- non-dystrophic genetic diseases of skeletal muscle, such as Spinal Muscular Atrophy and myopathies- maintenance of neuromuscular junctions- roles of ryanodine receptors and calcium signaling in skeletal muscle- roles of nuclear receptors in skeletal muscle- roles of GPCRs and GPCR signaling in skeletal muscle- other relevant aspects of skeletal muscle biology. In addition, articles on translational clinical studies that address molecular and cellular mechanisms of skeletal muscle will be published. Case reports are also encouraged for submission. Skeletal Muscle reflects the breadth of research on skeletal muscle and bridges gaps between diverse areas of science for example cardiac cell biology and neurobiology, which share common features with respect to cell differentiation, excitatory membranes, cell-cell communication, and maintenance. Suitable articles are model and mechanism-driven, and apply statistical principles where appropriate; purely descriptive studies are of lesser interest.
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