The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression. Issue 6 (21st February 2013)
- Record Type:
- Journal Article
- Title:
- The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression. Issue 6 (21st February 2013)
- Main Title:
- The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression
- Authors:
- Bertacchini, Jessika
Beretti, Francesca
Cenni, Vittoria
Guida, Marianna
Gibellini, Federica
Mediani, Laura
Marin, Oriano
Maraldi, Nadir M.
de Pol, Anto
Lattanzi, Giovanna
Cocco, Lucio
Marmiroli, Sandra - Abstract:
- Abstract : The serine/threonine kinase Akt/PKB is a major signaling hub integrating metabolic, survival, growth, and cell cycle regulatory signals. The definition of the phospho‐motif cipher driving phosphorylation by Akt led to the identification of hundreds of putative substrates, and it is therefore pivotal to identify those whose phosphorylation by Akt is of consequence to biological processes. The Lmna gene products lamin A/C and the lamin A precursor prelamin A are type V intermediate filament proteins forming a filamentous meshwork, the lamina, underneath the inner nuclear membrane, for nuclear envelope structures organization and interphase chromatin anchoring. In our previous work, we reported that A‐type lamins are phosphorylated by Akt at S301 and S404 in physiological conditions and are therefore bona fide substrates of Akt. We report here that Akt phosphorylation at S404 targets the precursor prelamin A for degradation. We further demonstrate that Akt also regulates Lmna transcription. Our study unveils a previously unknown function of Akt in the control of prelamin A stability and expression. Moreover, given the large number of diseases related to prelamin A, our findings represent a further important step bridging basic A‐type lamin physiology to therapeutic approaches for lamin A‐linked disorders.—Bertacchini, J., Beretti, F., Cenni, V., Guida, M., Gibellini, F., Mediani, L., Marin, O., Maraldi, N. M., de Pol, A., Lattanzi, G., Cocco, L., Marmiroli, S. TheAbstract : The serine/threonine kinase Akt/PKB is a major signaling hub integrating metabolic, survival, growth, and cell cycle regulatory signals. The definition of the phospho‐motif cipher driving phosphorylation by Akt led to the identification of hundreds of putative substrates, and it is therefore pivotal to identify those whose phosphorylation by Akt is of consequence to biological processes. The Lmna gene products lamin A/C and the lamin A precursor prelamin A are type V intermediate filament proteins forming a filamentous meshwork, the lamina, underneath the inner nuclear membrane, for nuclear envelope structures organization and interphase chromatin anchoring. In our previous work, we reported that A‐type lamins are phosphorylated by Akt at S301 and S404 in physiological conditions and are therefore bona fide substrates of Akt. We report here that Akt phosphorylation at S404 targets the precursor prelamin A for degradation. We further demonstrate that Akt also regulates Lmna transcription. Our study unveils a previously unknown function of Akt in the control of prelamin A stability and expression. Moreover, given the large number of diseases related to prelamin A, our findings represent a further important step bridging basic A‐type lamin physiology to therapeutic approaches for lamin A‐linked disorders.—Bertacchini, J., Beretti, F., Cenni, V., Guida, M., Gibellini, F., Mediani, L., Marin, O., Maraldi, N. M., de Pol, A., Lattanzi, G., Cocco, L., Marmiroli, S. The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression. FASEB J. 27, 2145–2155 (2013). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 27:Issue 6(2013)
- Journal:
- FASEB journal
- Issue:
- Volume 27:Issue 6(2013)
- Issue Display:
- Volume 27, Issue 6 (2013)
- Year:
- 2013
- Volume:
- 27
- Issue:
- 6
- Issue Sort Value:
- 2013-0027-0006-0000
- Page Start:
- 2145
- Page End:
- 2155
- Publication Date:
- 2013-02-21
- Subjects:
- 14.3.3 -- lamina phosphorylation -- nuclear signaling -- nucleus -- cell cycle
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.12-218214 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13220.xml