Helder Rocha
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Invited Adjunct Professor
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About
Helder Rocha is an Invited Adjunct Professor at the Polytechnic Institute of Porto, Portugal (+351). His research areas include cervical cancer prevention, evolutionary biology related to kinetochore size and chromosome alignment, as well as the regulation of organelle transport through interactions between JIP3 and motor proteins. His recent publications reflect a commitment to advancing knowledge in cancer prevention and cellular mechanics.
Recent Grants
Grant: Close
Axonal transport regulation by motor-cargo adaptors
Open Date: 2022-01-01
Close Date: 2025-01-01
Grant: Close
Molecular mechanisms of the dynein-dynactin transport machinery in health and disease
Open Date: 2018-07-01
Close Date: 2021-06-01
Grant: Close
Identification of Novel Conserved Dynein Pathway Genes Using a Genome-Wide Synthetic Lethal Screen in C. elegans
Open Date: 2015-03-01
Close Date: 2019-02-01
Grant: Close
Cytoplasmic Dynein: Mechanisms of Regulation and Novel Interactors
Open Date: 2014-03-01
Close Date: 2019-02-28
Grant: Close
Can polymorphism in the same set of genes explain within-species variation in life-history traits in divergent species?
Open Date: 2010-06-01
Close Date: 2013-11-30
Articles (4)
Year:
2025
Year:
2024
A landmark event in the transition from interphase to mitosis in metazoans is nuclear envelope breakdown (NEBD). Important mitotic events occur prior to NEBD, including condensation of replicated chromosomes and assembly of kinetochores to rapidly engage spindle microtubules. Here, we show that nuclear-enriched protein phosphatase 4 (PP4) ensures robust assembly of the microtubule-coupling outer kinetochore prior to NEBD. In the absence of PP4, chromosomes exhibit extended monopolar orientation after NEBD and subsequently mis-segregate. A secondary consequence of diminished outer kinetochore assembly is defective sister chromatid resolution. After NEBD, a cytoplasmic activity compensates for PP4 loss, leading to outer kinetochore assembly and recovery of chromosomes from monopolar orientation to significant bi-orientation. The Ndc80-Ska microtubule-binding module of the outer kinetochore is required for this recovery. PP4 associates with the inner kinetochore protein CENP-C; however, disrupting the PP4–CENP-C interaction does not perturb chromosome segregation. These results establish that PP4-dependent outer kinetochore assembly prior to NEBD is critical for timely and proper engagement of chromosomes with spindle microtubules.
Year:
2023
Year:
2022
Collaborators (5)
João H. Morais-Cabral
University of Porto
Daniel José Barbosa
Invited Assistant Professor
Cooperativa de Ensino Superior Politécnico e Universitário
Arshad Desai
University of California
Reto Gassmann
-
Ana X. Carvalho
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