CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Center for Ocean Mega-Science, Chinese Academy of Sciences, Qingdao 266404, China.
Laboratory for Marine Biology and Biotechnology, Qingdao Marine Science and Technology Center, Qingdao 266237, China.
Int J Mol Sci. 2024 Oct 2;25(19):10626. doi: 10.3390/ijms251910626.
In mammals, mixed lineage kinase domain-like protein (MLKL) is the executor of necroptosis. MLKL comprises an N-terminal domain (NTD), which alone suffices to trigger necroptosis by forming pores in the plasma membrane, and a C-terminal domain that inhibits the NTD activity. Evolutionarily, MLKL is poorly conserved in animals and not found in Protostomia. Although MLKL orthologs exist in invertebrate Deuterostomia, the biological activity of invertebrate MLKL is unknown. Herein, we examined 34 metazoan phyla and detected MLKL not only in Deuterostomia but also in Protostomia (Rotifera). The Rotifera MLKL exhibited low identities with non-Rotifera MLKL but shared relatively high identities with non-metazoan MLKL. In invertebrates, MLKL formed two phylogenetic clades, one of which was represented by Rotifera. In vertebrates, MLKL expression was tissue-specific and generally rich in immune organs. When expressed in human cells, the MLKL-NTD of Rotifera, Echinodermata, Urochordata, and Cephalochordata induced strong necroptosis. The necroptotic activity of Rotifera MLKL depended on a number of conserved residues. Together these findings provided new insights into the evolution of MLKL in Metazoa and revealed the biological activity of invertebrate MLKL.
在哺乳动物中,混合谱系激酶结构域样蛋白(MLKL)是坏死性凋亡的执行者。MLKL 由一个 N 端结构域(NTD)组成,该结构域本身足以通过在质膜上形成孔来触发坏死性凋亡,而 C 端结构域则抑制 NTD 的活性。在进化上,MLKL 在动物中保守性较差,在原生动物门中不存在。尽管后生动物门的无脊椎动物中有 MLKL 的同源物,但无脊椎动物 MLKL 的生物学活性尚不清楚。在此,我们研究了 34 个后生动物门,不仅在后生动物门中检测到 MLKL,而且在原生动物门(轮虫门)中也检测到 MLKL。轮虫 MLKL 与非轮虫 MLKL 的同源性较低,但与非后生动物的 MLKL 具有较高的同源性。在无脊椎动物中,MLKL 形成两个系统发育分支,其中一个分支由轮虫代表。在脊椎动物中,MLKL 的表达具有组织特异性,通常在免疫器官中丰富。当在人类细胞中表达时,轮虫、棘皮动物、尾索动物和头索动物的 MLKL-NTD 诱导强烈的坏死性凋亡。轮虫 MLKL 的坏死性凋亡活性依赖于一些保守残基。这些发现为后生动物门中 MLKL 的进化提供了新的见解,并揭示了无脊椎动物 MLKL 的生物学活性。