Document Detail


Small ubiquitin-like modifier-2 modification of retinoic acid receptor-alpha regulates its subcellular localization and transcriptional activity.
MedLine Citation:
PMID:  19850744     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The retinoic acid receptor-alpha (Rara) gene is critical for germ cell development in the testis, as demonstrated by infertile Rara knockout male mice. The encoded protein for Rara (RARA) is expressed in both Sertoli cells and germ cells, but it is not always in the nucleus. Previously, all-trans retinoic acid (ATRA) was shown to increase the nuclear localization and transcriptional activity of RARA in Sertoli cells. Here, we identified a small ubiquitin-like modifier-2 (SUMO-2) modification as a novel posttranslational regulatory mechanism controlling the ATRA-dependent RARA subcellular localization and transcription. ATRA increased the SUMO-2 modification of RARA. In the presence of ATRA, lysine 166 (K166) and K171 of RARA were modified at a physiological concentration of SUMO-2, whereas in the absence of ATRA, K399 was the only site that was modified, but at a higher SUMO-2 concentration. However, K399 was critical for ATRA-controlled nuclear trafficking of RARA. In the presence of ATRA, a K399 mutation to arginine resulted in the cytoplasmic localization of K399R mutant, indicating that K166 and K171 sumoylations were inhibitory to nuclear localization. This may be due to SUMO/sentrin-specific peptidase 6 (SENP6) not being able to bind K399R mutant to desumoylate K166 and K171 in Sertoli cells, whereas it can bind RARA with intact K399. On the other hand, functional K166 and K171 sites for sumoylation were required for a full transcriptional activity, when K399 was intact. These results together suggest that both K166 and K171 sumoylation and desumoylation are critical for optimal RARA function.
Authors:
Li Zhu; Nadine C Santos; Kwan Hee Kim
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2009-10-22
Journal Detail:
Title:  Endocrinology     Volume:  150     ISSN:  1945-7170     ISO Abbreviation:  Endocrinology     Publication Date:  2009 Dec 
Date Detail:
Created Date:  2009-11-25     Completed Date:  2010-01-19     Revised Date:  2011-08-01    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  United States    
Other Details:
Languages:  eng     Pagination:  5586-95     Citation Subset:  AIM; IM    
Affiliation:
School of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, Washington 99164, USA.
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MeSH Terms
Descriptor/Qualifier:
Amino Acid Sequence
Animals
Binding Sites / genetics
Blotting, Western
COS Cells
Cell Line
Cell Nucleus / drug effects,  metabolism
Cercopithecus aethiops
Humans
Lysine / genetics,  metabolism
Male
Molecular Sequence Data
Mutation
Protein Binding
Protein Processing, Post-Translational*
Rats
Rats, Sprague-Dawley
Receptors, Retinoic Acid / genetics,  metabolism*
Reverse Transcriptase Polymerase Chain Reaction
Sequence Homology, Amino Acid
Sertoli Cells / cytology,  metabolism
Small Ubiquitin-Related Modifier Proteins / genetics,  metabolism*
Transcriptional Activation / drug effects,  genetics*
Tretinoin / pharmacology
Grant Support
ID/Acronym/Agency:
HD44569/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/Receptors, Retinoic Acid; 0/SUMO2 protein, rat; 0/Small Ubiquitin-Related Modifier Proteins; 0/retinoic acid receptor alpha; 302-79-4/Tretinoin; 56-87-1/Lysine
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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