Micronuclei from misaligned chromosomes that satisfy the spindle assembly checkpoint in cancer cells

• Tipo: Artigo em Revista Científica Internacional
• Data: 2022

Autores

Gomes, AM (Autor) Outra; Orr, B (Autor) Outra; Novais Cruz, M (Autor) Outra; De Sousa, F (Autor) Outra; Macario Monteiro, J (Autor) Outra; Carolina Lemos (Autor) ICBAS; Ferras, C (Autor) Outra; Helder Maiato (Autor) FMUP

Revista

Título: Current Biology

Vol. 32

Páginas: 4240-+

ISSN: 0960-9822

Editora: Elsevier

Indexação

ISI Web of Knowledge - 7 Citações

Scopus - 6 Citações

Outras Informações

ID Authenticus: P-00X-B00

DOI: 10.1016/j.cub.2022.08.026

Abstract (EN): Chromosome alignment to the spindle equator is a hallmark of mitosis thought to promote chromosome segregation fidelity in metazoans. Yet chromosome alignment is only indirectly supervised by the spindle assembly checkpoint (SAC) as a byproduct of chromosome bi-orientation, and the consequences of defective chromosome alignment remain unclear. Here, we investigated how human cells respond to chromosome alignment defects of distinct molecular nature by following the fate of live HeLa cells after RNAi-mediated depletion of 125 proteins previously implicated in chromosome alignment. We confirmed chromosome alignment defects upon depletion of 108/125 proteins. Surprisingly, in all confirmed cases, depleted cells frequently entered anaphase after a delay with misaligned chromosomes. Using depletion of prototype proteins resulting in defective chromosome alignment, we show that misaligned chromosomes often satisfy the SAC and directly missegregate without lagging behind in anaphase. In-depth analysis of specific molecular perturbations that prevent proper kinetochore-microtubule attachments revealed that misaligned chromosomes that missegregate frequently result in micronuclei. Higher-resolution live-cell imaging indicated that, contrary to most anaphase lagging chromosomes that correct and reintegrate the main nuclei, misaligned chromosomes are a strong predictor of micronuclei formation in a cancer cell model of chromosomal instability, but not in non-transformed near-diploid cells. We provide evidence supporting that intrinsic differences in kinetochore-microtubule attachment stability on misaligned chromosomes account for this distinct outcome. Thus, misaligned chromosomes that satisfy the SAC may represent a previously over-looked mechanism driving chromosomal/genomic instability during cancer cell division, and we unveil genetic conditions predisposing for these events.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 21