TY - JOUR
T1 - Formin-mediated nuclear actin at androgen receptors promotes transcription
AU - Knerr, Julian
AU - Werner, Ralf
AU - Schwan, Carsten
AU - Wang, Hong
AU - Gebhardt, Peter
AU - Grötsch, Helga
AU - Caliebe, Almuth
AU - Spielmann, Malte
AU - Holterhus, Paul Martin
AU - Grosse, Robert
AU - Hornig, Nadine C.
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2023/5/18
Y1 - 2023/5/18
N2 - Steroid hormone receptors are ligand-binding transcription factors essential for mammalian physiology. The androgen receptor (AR) binds androgens mediating gene expression for sexual, somatic and behavioural functions, and is involved in various conditions including androgen insensitivity syndrome and prostate cancer1. Here we identified functional mutations in the formin and actin nucleator DAAM2 in patients with androgen insensitivity syndrome. DAAM2 was enriched in the nucleus, where its localization correlated with that of the AR to form actin-dependent transcriptional droplets in response to dihydrotestosterone. DAAM2 AR droplets ranged from 0.02 to 0.06 µm3 in size and associated with active RNA polymerase II. DAAM2 polymerized actin directly at the AR to promote droplet coalescence in a highly dynamic manner, and nuclear actin polymerization is required for prostate-specific antigen expression in cancer cells. Our data uncover signal-regulated nuclear actin assembly at a steroid hormone receptor necessary for transcription.
AB - Steroid hormone receptors are ligand-binding transcription factors essential for mammalian physiology. The androgen receptor (AR) binds androgens mediating gene expression for sexual, somatic and behavioural functions, and is involved in various conditions including androgen insensitivity syndrome and prostate cancer1. Here we identified functional mutations in the formin and actin nucleator DAAM2 in patients with androgen insensitivity syndrome. DAAM2 was enriched in the nucleus, where its localization correlated with that of the AR to form actin-dependent transcriptional droplets in response to dihydrotestosterone. DAAM2 AR droplets ranged from 0.02 to 0.06 µm3 in size and associated with active RNA polymerase II. DAAM2 polymerized actin directly at the AR to promote droplet coalescence in a highly dynamic manner, and nuclear actin polymerization is required for prostate-specific antigen expression in cancer cells. Our data uncover signal-regulated nuclear actin assembly at a steroid hormone receptor necessary for transcription.
UR - http://www.scopus.com/inward/record.url?scp=85159141811&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/43247458-6aff-337d-b024-05387e46f9c7/
U2 - 10.1038/s41586-023-05981-1
DO - 10.1038/s41586-023-05981-1
M3 - Journal articles
C2 - 36972684
AN - SCOPUS:85159141811
SN - 0028-0836
VL - 617
SP - 616
EP - 622
JO - Nature
JF - Nature
IS - 7961
ER -