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This version published online on October 19, 2006
Endocrinology, doi:10.1210/en.2006-0660
A more recent version of this article appeared on January 1, 2007
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Submitted on May 16, 2006
Accepted on October 10, 2006

THYROID HORMONES INDUCE SUMOYLATION OF THE COLD SHOCK DOMAIN-CONTAINING PROTEIN PIPPIN IN DEVELOPING RAT BRAIN AND IN CULTURED NEURONS

Epifania Bono, Vincenza Compagno, Patrizia Proia, Lavinia Raimondi, Gabriella Schiera, Vincenzo Favaloro, Valerio Campo, Maria Donatelli, and Italia Di Liegro*

Dipartimento di Biologia Cellulare e dello Sviluppo ‘Alberto Monroy’, Dipartimento Biomedico di Medicina Interna e Specialistiche, Dipartimento di Neurologia, Oftalmologia, Otorinolaringoiatria e Psichiatria, and Dipartimento di Scienze Biochimiche, University of Palermo, Palermo, Italy

* To whom correspondence should be addressed. E-mail: diliegro{at}unipa.it.

We previously identified a cold shock domain (CSD)-containing protein (PIPPin), expressed at high level in brain cells. PIPPin has the potential to undergo different post-translational modifications and might be a good candidate to regulate the synthesis of specific proteins in response to extracellular stimuli. Here we report the effects of thyroid hormone (T3) on PIPPin expression in developing rat brain. We found that a significant difference among euthyroid- and hypothyroid- newborn rats concerns sumoylation of nuclear PIPPin, that is abolished by hypothyroidism. Moreover, T3-dependence of PIPPin sumoylation has been confirmed in cortical neurons purified from brain cortices and cultured in a chemically defined medium (Maat medium, MM), with or without T3. We also report that about one half of unmodified as well as all the sumoylated form of PIPPin could be extracted from nuclei with HCl, together with histones. Moreover, this HCl-soluble fraction remains in the nucleus even after treatment with 0.6 M KCl, thus suggesting strong interaction of PIPPin with nuclear structures and perhaps chromatin.


Key words: thyroid hormones • PIPPin • sumoylation







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