Analysis of the assembly, stabilization and maturation of the multiphasic TAZ biomolecular condensates

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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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Abstract

ABSTRACT Phase separation is an important mechanism ensuring efficient regulation and function in Hippo signaling. Particularly, phase separation of nuclear TAZ has been demonstrated to be essential for its activity. However, the mechanisms of TAZ condensate assembly and maturation are yet undefined. Here we explored these mechanisms using FRAP with two laser beam sizes complemented by microscopy and cell biology approaches. We show that TAZ condensates are multiphasic, with a more stable core and labile periphery. TAZ initially forms small nascent clusters, likely via self-nucleation through the CC domain. These gradually mature into larger condensates through interaction with additional proteins via the WW domain. The condensates are further stabilized/activated by interaction with transcription factors and complexes including TEAD4 and P-TEFb. Of note, the ability of TAZ to form mature condensates is essential for its activities in cellular morphogenesis and tumorigenesis. Our study presents detailed mechanistic analysis of TAZ phase separation, revealing a highly dynamic nature of TAZ condensate maturation and activation. Teaser TAZ condensates grow from nascent clusters into mature condensates by interactions with transcription factors and complexes.
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ABSTRACT Phase separation is an important mechanism ensuring efficient regulation and function in Hippo signaling. Particularly, phase separation of nuclear TAZ has been demonstrated to be essential for its activity. However, the mechanisms of TAZ condensate assembly and maturation are yet undefined. Here we explored these mechanisms using FRAP with two laser beam sizes complemented by microscopy and cell biology approaches. We show that TAZ condensates are multiphasic, with a more stable core and labile periphery. TAZ initially forms small nascent clusters, likely via self-nucleation through the CC domain. These gradually mature into larger condensates through interaction with additional proteins via the WW domain. The condensates are further stabilized/activated by interaction with transcription factors and complexes including TEAD4 and P-TEFb. Of note, the ability of TAZ to form mature condensates is essential for its activities in cellular morphogenesis and tumorigenesis. Our study presents detailed mechanistic analysis of TAZ phase separation, revealing a highly dynamic nature of TAZ condensate maturation and activation. Teaser TAZ condensates grow from nascent clusters into mature condensates by interactions with transcription factors and complexes. Competing Interest Statement The authors have declared no competing interest.

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last seen: 2026-05-20T01:45:00.602351+00:00