Zhang Haifeng, Shang Renjie, Kim Kwantae, Zheng Wei, Johnson Christopher J, Sun Lei, Niu Xiang, Liu Liang, Zhou Jingqi, Liu Lingshu, Zhang Zheng, Uyeno Theodore A, Pei Jimin, Fissette Skye D, Green Stephen A, Samudra Sukhada P, Wen Junfei, Zhang Jianli, Eggenschwiler Jonathan T, Menke Douglas B, Bronner Marianne E, Grishin Nick V, Li Weiming, Ye Kaixiong, Zhang Yang, Stolfi Alberto, Bi Pengpeng
Center for Molecular Medicine, University of Georgia, Athens, GA, USA.
Department of Genetics, University of Georgia, Athens, GA, USA.
Sci Adv. 2022 Sep 2;8(35):eadd2696. doi: 10.1126/sciadv.add2696.
Vertebrate myoblast fusion allows for multinucleated muscle fibers to compound the size and strength of mononucleated cells, but the evolution of this important process is unknown. We investigated the evolutionary origins and function of membrane-coalescing agents Myomaker and Myomixer in various groups of chordates. Here, we report that likely arose through gene duplication in the last common ancestor of tunicates and vertebrates, while appears to have evolved de novo in early vertebrates. Functional tests revealed a complex evolutionary history of myoblast fusion. A prevertebrate phase of muscle multinucleation driven by Myomaker was followed by the later emergence of Myomixer that enables the highly efficient fusion system of vertebrates. Evolutionary comparisons between vertebrate and nonvertebrate Myomaker revealed key structural and mechanistic insights into myoblast fusion. Thus, our findings suggest an evolutionary model of chordate fusogens and illustrate how new genes shape the emergence of novel morphogenetic traits and mechanisms.
脊椎动物的成肌细胞融合使得多核肌纤维能够增强单核细胞的大小和力量,但这一重要过程的进化情况尚不清楚。我们研究了膜融合因子肌生成素(Myomaker)和肌融合素(Myomixer)在各种脊索动物群体中的进化起源和功能。在此,我们报告称,肌生成素可能是通过被囊动物和脊椎动物的最后一个共同祖先中的基因复制产生的,而肌融合素似乎是在早期脊椎动物中从头进化而来的。功能测试揭示了成肌细胞融合复杂的进化历史。由肌生成素驱动的肌肉多核化的脊椎动物前阶段之后,肌融合素出现,从而形成了脊椎动物高效的融合系统。脊椎动物和非脊椎动物的肌生成素之间的进化比较揭示了成肌细胞融合的关键结构和机制见解。因此,我们的研究结果提出了一种脊索动物融合蛋白的进化模型,并说明了新基因如何塑造新的形态发生特征和机制的出现。