Analysis of the assembly, stabilization and maturation of the multiphasic TAZ biomolecular condensates
This study reveals that TAZ condensates assemble from nascent clusters into multiphasic structures with stable cores and labile peripheries, maturing through interactions with proteins and transcription factors.
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The paper investigates how nuclear TAZ biomolecular condensates assemble, mature, and become stabilized in the context of Hippo signaling, using FRAP with two laser beam sizes along with microscopy and cell biology. The authors find that TAZ condensates are multiphasic, featuring a stable core and a more labile periphery, and that TAZ first forms small nascent clusters likely via self-nucleation through the CC domain, which then mature into larger condensates through interactions mediated by the WW domain with additional proteins. Further stabilization and activation are attributed to interactions involving transcription factors and complexes including TEAD4 and P-TEFb, and the ability to form mature condensates is reported as essential for TAZ activities in cellular morphogenesis and tumorigenesis. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.
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- last seen: 2026-05-20T01:45:00.602351+00:00