4.8 Article

Gene replacement strategies validate the use of functional tags on centromeric chromatin and invalidate an essential role for CENP-AK124ub

Journal

CELL REPORTS
Volume 37, Issue 5, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2021.109924

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Funding

  1. Centre National de la Recherche Scientifique (CNRS, France)
  2. National Institutes of Health (NIH, USA) [R35GM130302]
  3. Agence Nationale de la Recherche (ANR, France) [ANR-18-ERC1-0004-01, ANR-19CE12-0022]
  4. Labex <> [ANR-10LABX-0038, ANR-10-IDEX-0001-02]
  5. Agence Nationale de la Recherche (ANR) [ANR-18-ERC1-0004] Funding Source: Agence Nationale de la Recherche (ANR)

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Functional tags are widely used in cell biology, with the centromere being a particularly useful locus for such studies. Regulation of centromere function involves posttranslational modification of key components, including CENP-A. Some have questioned the effectiveness of functional tags in studying the essentiality of specific posttranslational modifications, such as CENP-A(K124) ubiquitination.
Functional tags are ubiquitous in cell biology, and for studies of one chromosomal locus, the centromere, tags have been remarkably useful. The centromere directs chromosome inheritance at cell division. The location of the centromere is defined by a histone H3 variant, CENP-A. The regulation of the chromatin assembly pathway essential for centromere inheritance and function includes posttranslational modification (PTM) of key components, including CENP-A itself. Others have recently called into question the use of functional tags, with the claim that at least two widely used tags obscured the essentiality of one particular PTM, CENP-A(K124) ubiquitination (ub). Here, we employ three independent gene replacement strategies that eliminate large, lysine-containing tags to interrogate these claims. Using these approaches, we find no evidence to support an essential function of CENP-A(K124ub). Our general methodology will be useful to validate discoveries permitted by powerful functional tagging schemes at the centromere and other cellular locations.

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