DNA ‐binding domain as the minimal region driving RNA ‐dependent liquid‐liquid phase separation of androgen receptor

2021 ◽  
Author(s):  
Junaid Ahmed ◽  
Attila Meszaros ◽  
Tamas Lazar ◽  
Peter Tompa
Keyword(s):  
Phase Separation ◽  
Androgen Receptor ◽  
Liquid Phase ◽  
Dna Binding ◽  
Binding Domain ◽  
Liquid Phase Separation ◽  
Dna Binding Domain ◽  
Liquid Liquid Phase Separation ◽  
Minimal Region

scholarly journals Aggresome Formation and Liquid-liquid Phase Separation Independently Induce Cytoplasmic Aggregation of TAR DNA-binding protein 43

2020 ◽  
Author(s):  
Koji Yamanaka ◽  
Seiji Watanabe ◽  
Hidekazu Inami ◽  
Kotaro Oiwa ◽  
Yuri Murata ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Dna Binding ◽  
Binding Protein ◽  
Dna Binding Protein ◽  
Liquid Phase Separation ◽  
Mammalian Expression ◽  
Sporadic Als ◽  
Aggresome Formation ◽  
Liquid Liquid Phase Separation

Abstract Background Cytoplasmic inclusion of TAR DNA-binding protein 43 (TDP-43) is a pathological hallmark of amyotrophic lateral sclerosis (ALS) and a subtype of frontotemporal lobar degeneration (FTLD). Recent studies have suggested that the formation of cytoplasmic TDP-43 aggregates is dependent on a liquid-liquid phase separation (LLPS) mechanism. However, it is unclear whether TDP-43 pathology is induced through a single intracellular mechanism such as LLPS.Methods We established a TDP-43 aggregation screening system using a cultured neuronal cell line stably expressing EGFP-fused TDP-43 and a mammalian expression library of the inherited ALS/FTLD causative genes. We performed a screening to identify the intracellular mechanisms responsible for TDP-43 aggregation. An immunofluorescence study was conducted using the sporadic ALS spinal cord sections.Results We found that microtubule-related proteins (MRPs) and RNA-binding proteins (RBPs) co-aggregated with TDP-43. MRPs and RBPs sequestered TDP-43 into the cytoplasmic aggregates through distinct mechanisms such as microtubules and LLPS, respectively. The MRPs-induced TDP-43 aggregates were co-localized with aggresomal markers and dependent on histone deacetylase 6 (HDAC6), suggesting that aggresome formation induced the co-aggregation. However, the MRPs-induced aggregates were not affected by 1,6-hexanediol, an LLPS inhibitor. On the other hand, the RBPs-induced TDP-43 aggregates were sensitive to 1,6-hexanediol, but not dependent on microtubules or HDAC6. In sporadic ALS patients, approximately half of skein-like TDP-43 inclusions were co-localized with HDAC6, but round and granular type inclusion were not. Moreover, HDAC6-positive and HDAC6-negative inclusions were found in the same ALS patient, suggesting that the two distinct pathways are both involved in TDP-43 pathology.Conclusion Our findings suggest that at least two distinct pathways (i.e., aggresome formation and LLPS ) are involved in inducing the TDP-43 pathologies.

scholarly journals Poly-glutamine-dependent self-association as a potential mechanism for regulation of androgen receptor activity

2021 ◽  
Author(s):  
Josep Rizo ◽  
Carlos M. Roggero ◽  
Victoria Esser ◽  
Lingling Duan ◽  
Allyson M. Rice ◽  
...  
Keyword(s):  
Prostate Cancer ◽  
Phase Separation ◽  
Androgen Receptor ◽  
Liquid Phase ◽  
Transcriptional Activity ◽  
Molecular Mechanisms ◽  
Catalytic Domain ◽  
Low Complexity ◽  
Liquid Phase Separation ◽  
Liquid Liquid Phase Separation

The androgen receptor (AR) plays a central role in prostate cancer. Development of castration resistant prostate cancer (CRPC) requires androgen-independent activation of AR, which involves its large N-terminal domain (NTD) and entails dramatic epigenetic changes depending in part on histone lysine demethylases (KDMs) that interact with AR. The AR-NTD is rich in low-complexity sequences, including a polyQ repeat. Longer polyQ sequences were reported to decrease transcriptional activity and to protect against prostate cancer. However, the molecular mechanisms underlying these observations are unclear. Using NMR spectroscopy, here we identify weak interactions between the AR-NTD and the KDM4A catalytic domain, and between the AR ligand-binding domain and a central KDM4A region that also contains low-complexity sequences. We also show that the AR-NTD can undergo liquid-liquid phase separation in vitro, with longer polyQ sequences phase separating more readily. Moreover, longer polyQ sequences hinder nuclear localization in the absence of hormone and increase the propensity for formation of AR-containing puncta in the nucleus of cells treated with dihydrotestosterone. These results lead us to hypothesize that polyQ-dependent liquid-liquid phase separation may provide a mechanism to decrease the transcriptional activity of AR, potentially opening new opportunities to design effective therapies against CRPC.

scholarly journals Aggresome formation and liquid–liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43

2020 ◽  
Vol 11 (10) ◽  
Author(s):  
Seiji Watanabe ◽  
Hidekazu Inami ◽  
Kotaro Oiwa ◽  
Yuri Murata ◽  
Shohei Sakai ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Dna Binding ◽  
Binding Protein ◽  
Dna Binding Protein ◽  
Liquid Phase Separation ◽  
Mammalian Expression ◽  
Sporadic Als ◽  
Aggresome Formation ◽  
Liquid Liquid Phase Separation

Abstract Cytoplasmic inclusion of TAR DNA-binding protein 43 (TDP-43) is a pathological hallmark of amyotrophic lateral sclerosis (ALS) and a subtype of frontotemporal lobar degeneration (FTLD). Recent studies have suggested that the formation of cytoplasmic TDP-43 aggregates is dependent on a liquid–liquid phase separation (LLPS) mechanism. However, it is unclear whether TDP-43 pathology is induced through a single intracellular mechanism such as LLPS. To identify intracellular mechanisms responsible for TDP-43 aggregation, we established a TDP-43 aggregation screening system using a cultured neuronal cell line stably expressing EGFP-fused TDP-43 and a mammalian expression library of the inherited ALS/FTLD causative genes, and performed a screening. We found that microtubule-related proteins (MRPs) and RNA-binding proteins (RBPs) co-aggregated with TDP-43. MRPs and RBPs sequestered TDP-43 into the cytoplasmic aggregates through distinct mechanisms, such as microtubules and LLPS, respectively. The MRPs-induced TDP-43 aggregates were co-localized with aggresomal markers and dependent on histone deacetylase 6 (HDAC6), suggesting that aggresome formation induced the co-aggregation. However, the MRPs-induced aggregates were not affected by 1,6-hexanediol, an LLPS inhibitor. On the other hand, the RBPs-induced TDP-43 aggregates were sensitive to 1,6-hexanediol, but not dependent on microtubules or HDAC6. In sporadic ALS patients, approximately half of skein-like TDP-43 inclusions were co-localized with HDAC6, but round and granular type inclusion were not. Moreover, HDAC6-positive and HDAC6-negative inclusions were found in the same ALS patient, suggesting that the two distinct pathways are both involved in TDP-43 pathology. Our findings suggest that at least two distinct pathways (i.e., aggresome formation and LLPS) are involved in inducing the TDP-43 pathologies.

scholarly journals Poly-glutamine-dependent self-association as a potential mechanism for regulation of androgen receptor activity

PLoS ONE ◽  
2022 ◽  
Vol 17 (1) ◽  
pp. e0258876
Author(s):  
Carlos M. Roggero ◽  
Victoria Esser ◽  
Lingling Duan ◽  
Allyson M. Rice ◽  
Shihong Ma ◽  
...  
Keyword(s):  
Prostate Cancer ◽  
Phase Separation ◽  
Androgen Receptor ◽  
Liquid Phase ◽  
Transcriptional Activity ◽  
Molecular Mechanisms ◽  
Muscular Atrophy ◽  
Low Complexity ◽  
Liquid Phase Separation ◽  
Liquid Liquid Phase Separation

The androgen receptor (AR) plays a central role in prostate cancer. Development of castration resistant prostate cancer (CRPC) requires androgen-independent activation of AR, which involves its large N-terminal domain (NTD) and entails extensive epigenetic changes depending in part on histone lysine demethylases (KDMs) that interact with AR. The AR-NTD is rich in low-complexity sequences, including a polyQ repeat. Longer polyQ sequences were reported to decrease transcriptional activity and to protect against prostate cancer, although they can lead to muscular atrophy. However, the molecular mechanisms underlying these observations are unclear. Using NMR spectroscopy, here we identify weak interactions between the AR-NTD and the KDM4A catalytic domain, and between the AR ligand-binding domain and a central KDM4A region that also contains low-complexity sequences. We also show that the AR-NTD can undergo liquid-liquid phase separation in vitro, with longer polyQ sequences phase separating more readily. Moreover, longer polyQ sequences hinder nuclear localization in the absence of hormone and increase the propensity for formation of AR-containing puncta in the nucleus of cells treated with dihydrotestosterone. These results lead us to hypothesize that polyQ-dependent liquid-liquid phase separation may provide a mechanism to decrease the transcriptional activity of AR, potentially opening new opportunities to design effective therapies against CRPC and muscular atrophy.

scholarly journals TAR DNA-binding protein 43 (TDP-43) liquid–liquid phase separation is mediated by just a few aromatic residues

2018 ◽  
Vol 293 (16) ◽  
pp. 6090-6098 ◽  
Author(s):  
Hao-Ru Li ◽  
Wan-Chin Chiang ◽  
Po-Chun Chou ◽  
Won-Jing Wang ◽  
Jie-rong Huang
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Dna Binding ◽  
Binding Protein ◽  
Dna Binding Protein ◽  
Liquid Phase Separation ◽  
Aromatic Residues ◽  
Liquid Liquid Phase Separation

scholarly journals Liquid-Liquid Phase Separation of Tau Driven by Hydrophobic Interaction Facilitates Fibrillization of Tau

2021 ◽  
Vol 433 (2) ◽  
pp. 166731
Author(s):  
Yanxian Lin ◽  
Yann Fichou ◽  
Andrew P. Longhini ◽  
Luana C. Llanes ◽  
Pengyi Yin ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Hydrophobic Interaction ◽  
Liquid Phase Separation ◽  
Liquid Liquid Phase Separation

scholarly journals Amyloid Aggregation under the Lens of Liquid–Liquid Phase Separation

2020 ◽  
pp. 368-378
Author(s):  
Yanting Xing ◽  
Aparna Nandakumar ◽  
Aleksandr Kakinen ◽  
Yunxiang Sun ◽  
Thomas P. Davis ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Liquid Phase Separation ◽  
Amyloid Aggregation ◽  
Liquid Liquid Phase Separation
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