Identification and inhibition of the Cyclin D Rb-docking interface that drives cell division

The animal cell division cycle is initiated by the cyclin-dependent kinases CDK4 and CDK6 in complex with D-type cyclins. Cyclin D-CDK4/6 complex formation is promoted by the assembly factors p21 and p27, which bind both subunits. p27 binds the hydrophobic patch on cyclin D that is similar to the patch used by other cell cycle cyclins to dock their substrates. This raised the question as to how cyclin D could find its substrates if its hydrophobic patch were already occupied? Here, we show that D-type cyclins use their A2' helix to dock the retinoblastoma protein Rb, a key substrate regulating cell cycle progression. The specific interface of cyclin D's A2' helix is unique among cyclins and its mutation slows proliferation. Taken together, our work identifies a cyclin D-substrate docking mechanism that can be targeted by novel cancer therapeutics.

Authors

Institutions

Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-15
DOI
https://doi.org/10.64898/2026.01.14.699544
Primary Topic
Cancer-related Molecular Pathways
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Identification and inhibition of the Cyclin D Rb-docking interface that drives cell division

Ioannis Sanidas, Mardo Kõivomägi, Jan Marcel Skotheim, Michael C. Lanz et al.
bioRxiv (Cold Spring Harbor Laboratory)
Cancer-related Molecular Pathways
article

Identification and inhibition of the Cyclin D Rb-docking interface that drives cell division

Ioannis Sanidas, Mardo Kõivomägi, Jan Marcel Skotheim, Michael C. Lanz, Jürgen Tuvikene, Shuyuan Zhang, Julien Sage, Cecelia Fleming, Shicong Xie, Aiden Weaver, Benjamin Reyes Topacio, Seth Rubin
article en

Abstract

The animal cell division cycle is initiated by the cyclin-dependent kinases CDK4 and CDK6 in complex with D-type cyclins. Cyclin D-CDK4/6 complex formation is promoted by the assembly factors p21 and p27, which bind both subunits. p27 binds the hydrophobic patch on cyclin D that is similar to the patch used by other cell cycle cyclins to dock their substrates. This raised the question as to how cyclin D could find its substrates if its hydrophobic patch were already occupied? Here, we show that D-type cyclins use their A2' helix to dock the retinoblastoma protein Rb, a key substrate regulating cell cycle progression. The specific interface of cyclin D's A2' helix is unique among cyclins and its mutation slows proliferation. Taken together, our work identifies a cyclin D-substrate docking mechanism that can be targeted by novel cancer therapeutics.

bioRxiv (Cold Spring Harbor Laboratory)
National Institutes of Health (US), University of California, Santa Cruz (US), Massachusetts General Hospital (US), Chan Zuckerberg Initiative (United States) (US), National Cancer Institute (US), Pediatrics and Genetics (US), Center for Cancer Research (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 87%
Cancer-related Molecular Pathways
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.