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MEL-28/ELYS and CENP-C coordinately control outer kinetochore assembly and meiotic chromosome-microtubule interactions.
- Source :
-
Current biology : CB [Curr Biol] 2022 Jun 06; Vol. 32 (11), pp. 2563-2571.e4. Date of Electronic Publication: 2022 May 23. - Publication Year :
- 2022
-
Abstract
- During mitosis and meiosis in the majority of eukaryotes, centromeric chromatin comprised of CENP-A nucleosomes and their reader CENP-C recruits components of the outer kinetochore to build an interface with spindle microtubules. <superscript>1</superscript> <superscript>,</superscript> <superscript>2</superscript> One exception is C. elegans oocyte meiosis, where outer kinetochore proteins form cup-like structures on chromosomes independently of centromeric chromatin. <superscript>3</superscript> Here, we show that the nucleoporin MEL-28 (ortholog of human ELYS) and CENP-C <superscript>HCP-4</superscript> act in parallel to recruit outer kinetochore components to oocyte meiotic chromosomes. Unexpectedly, co-inhibition of MEL-28 and CENP-C <superscript>HCP-4</superscript> resulted in chromosomes being expelled from the meiotic spindle prior to anaphase onset, a more severe phenotype than what was observed following ablation of the outer kinetochore. <superscript>4</superscript> <superscript>,</superscript> <superscript>5</superscript> This observation suggested that MEL-28 and the outer kinetochore independently link chromosomes to spindle microtubules. Consistent with this, the chromosome expulsion defect was observed following co-inhibition of MEL-28 and the microtubule-coupling KNL-1/MIS-12/NDC-80 (KMN) network of the outer kinetochore. Use of engineered mutants showed that MEL-28 acts in conjunction with the microtubule-binding NDC-80 complex to keep chromosomes within the oocyte meiotic spindle and that this function likely involves the Y-complex of nucleoporins that associate with MEL-28; by contrast, the ability to dock protein phosphatase 1, shared by MEL-28 and KNL-1, is not involved. These results highlight nuclear pore-independent functions for a conserved nucleoporin and explain two unusual features of oocyte meiotic chromosome segregation in C. elegans: centromeric chromatin-independent outer kinetochore assembly, and dispensability of the outer kinetochore for constraining chromosomes in the acentrosomal meiotic spindle.<br />Competing Interests: Declaration of interests N.H. is currently an employee of AstraZeneca.<br /> (Copyright © 2022 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Caenorhabditis elegans physiology
Chromatin metabolism
Chromosomal Proteins, Non-Histone
Chromosome Segregation
DNA-Binding Proteins metabolism
Microtubule-Associated Proteins metabolism
Microtubules metabolism
Mitosis
Nuclear Pore Complex Proteins metabolism
Spindle Apparatus metabolism
Caenorhabditis elegans Proteins genetics
Caenorhabditis elegans Proteins metabolism
Kinetochores metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0445
- Volume :
- 32
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Current biology : CB
- Publication Type :
- Academic Journal
- Accession number :
- 35609608
- Full Text :
- https://doi.org/10.1016/j.cub.2022.04.046