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Methyl CpG binding protein 2 (MeCP2) is a chromatin-associated protein that remains enigmatic despite more than 30 years of research, primarily due to the ever-growing list of its molecular functions, and, consequently, its related pathologies. Loss of function MECP2 mutations cause the neurodevelopmental disorder Rett syndrome (RTT); in addition, dysregulation of MeCP2 expression and/or function are involved in numerous other pathologies, but the mechanisms of MeCP2 regulation are unclear. Advancing technologies and burgeoning mechanistic theories assist our understanding of the complexity of MeCP2 but may inadvertently cloud it if not rigorously tested.

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The early Cambrian is a non-feeding larva of a scalidophoran worm.

Proc Biol Sci

December 2024

Université de Lyon, Université Claude Bernard Lyon 1, ENS Lyon, CNRS UMR 5276, Laboratoire de géologie de Lyon: Terre, Planètes, Environnement, Bâtiment GEODE, Villeurbanne 69622, France.

With its bag-like appearance, spiny ornament and single opening, is one of the most enigmatic animals of the early Cambrian Kuanchuanpu Formation ( 535 Ma) and has been at the heart of debates concerning the origin of two major animal lineages: the deuterostomes and the ecdysozoans. Although Ecdysozoa is now the most plausible option, key aspects of its palaeobiology have remained elusive. I suggest here that was the possible larval stage of one of the numerous scalidophoran worms that co-existed with it in the Kuanchuanpu biota, especially those with bilateral pairs of broad-based sclerites such as .

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