The cohesion establishment factor Esco1 acetylates ?-tubulin to ensure proper spindle assembly in oocyte meiosis.

ABSTRACT: Esco1 has been reported to function as a cohesion establishment factor that mediates chromosome cohesion and segregation in mitotic cells. However, its exact roles in meiosis have not been clearly defined. Here, we document that Esco1 is expressed and localized to both the nucleus and cytoplasm during mouse oocyte meiotic maturation. Depletion of Esco1 by siRNA microinjection causes the meiotic progression arrest with a severe spindle abnormality and chromosome misalignment, which is coupled with a higher incidence of the erroneous kinetochore-microtubule attachments and activation of spindle assembly checkpoint. In addition, depletion of Esco1 leads to the impaired microtubule stability shown by the weakened resistance ability to the microtubule depolymerizing drug nocodazole and the decreased level of acetylated ?-tubulin. Conversely, overexpression of Esco1 causes hyperacetylation of ?-tubulin and spindle defects. Moreover, we find that Esco1 binds to ?-tubulin and is required for its acetylation. The reduced acetylation level of ?-tubulin in Esco1-depleted oocytes can be restored by the ectopic expression of exogenous wild-type Esco1 but not enzymatically dead Esco1-G768D. Purified wild-type Esco1 instead of mutant Esco1-G768D acetylates the synthesized peptide of ?-tubulin in vitro. Collectively, our data assign a novel function to Esco1 as a microtubule regulator during oocyte meiotic maturation beyond its conventional role in chromosome cohesion.

SUBMITTER: Lu Y 

PROVIDER: S-EPMC5861441 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature