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脊椎动物中必需和兼性肌肉多核化的顺式调控逻辑的变化。

A change in cis-regulatory logic underlying obligate versus facultative muscle multinucleation in chordates.

机构信息

School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332, USA.

Department of Genetics, University of Georgia, Athens, GA 30602, USA.

出版信息

Development. 2024 Oct 15;151(20). doi: 10.1242/dev.202968. Epub 2024 Sep 3.

Abstract

Vertebrates and tunicates are sister groups that share a common fusogenic factor, Myomaker (Mymk), that drives myoblast fusion and muscle multinucleation. Yet they are divergent in when and where they express Mymk. In vertebrates, all developing skeletal muscles express Mymk and are obligately multinucleated. In tunicates, Mymk is expressed only in post-metamorphic multinucleated muscles, but is absent from mononucleated larval muscles. In this study, we demonstrate that cis-regulatory sequence differences in the promoter region of Mymk underlie the different spatiotemporal patterns of its transcriptional activation in tunicates and vertebrates. Although in vertebrates myogenic regulatory factors (MRFs) such as MyoD1 alone are required and sufficient for Mymk transcription in all skeletal muscles, we show that transcription of Mymk in post-metamorphic muscles of the tunicate Ciona requires the combinatorial activity of MRF, MyoD and Early B-cell Factor (Ebf). This macroevolutionary difference appears to be encoded in cis, likely due to the presence of a putative Ebf-binding site adjacent to predicted MRF binding sites in the Ciona Mymk promoter. We further discuss how Mymk and myoblast fusion might have been regulated in the last common ancestor of tunicates and vertebrates, for which we propose two models.

摘要

脊椎动物和被囊动物是姐妹群,它们具有共同的融合因子 Myomaker (Mymk),该因子驱动成肌细胞融合和肌肉多核化。然而,它们在何时何地表达 Mymk 方面存在差异。在脊椎动物中,所有发育中的骨骼肌都表达 Mymk 并被迫多核化。在被囊动物中,Mymk 仅在变态后的多核化肌肉中表达,但在单核化的幼虫肌肉中不存在。在这项研究中,我们证明了 Mymk 启动子区域的顺式调控序列差异是导致其在被囊动物和脊椎动物中不同时空转录激活模式的基础。尽管在脊椎动物中,肌调节因子(MRF)如 MyoD1 单独对于所有骨骼肌中 Mymk 的转录是必需且充分的,但我们表明,被囊动物 Ciona 变态后肌肉中 Mymk 的转录需要 MRF、MyoD 和早期 B 细胞因子(Ebf)的组合活性。这种宏观进化差异似乎是顺式编码的,可能是由于在 Ciona Mymk 启动子中紧邻预测的 MRF 结合位点存在一个假定的 Ebf 结合位点。我们进一步讨论了 Mymk 和成肌细胞融合在被囊动物和脊椎动物的最后共同祖先中是如何被调控的,为此我们提出了两种模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a9a/11441980/209b1e40a393/develop-151-202968-g1.jpg

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