Expression of human Bcl-xL (Ser49) and (Ser62) mutants in Caenorhabditis elegans causes germline defects and aneuploidy.
An interesting feature of Bcl-xL protein is the presence of an unstructured loop domain between α1 and α2 helices, a domain not essential for its anti-apoptotic function and absent in CED-9 protein. Within this domain, Bcl-xL undergoes dynamic phosphorylation and dephosphorylation at Ser49 and Ser62...
Main Authors: | Prasamit Saurav Baruah, Myriam Beauchemin, J Alexander Parker, Richard Bertrand |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2017-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC5421811?pdf=render |
Similar Items
-
Dynamic Bcl-xL (S49) and (S62) Phosphorylation/Dephosphorylation during Mitosis Prevents Chromosome Instability and Aneuploidy in Normal Human Diploid Fibroblasts.
by: Prasamit Saurav Baruah, et al.
Published: (2016-01-01) -
Ser14 phosphorylation of Bcl-xL mediates compensatory cardiac hypertrophy in male mice
by: Michinari Nakamura, et al.
Published: (2023-09-01) -
An Aneuploidy-Free and Structurally Defined Balancer Chromosome Toolkit for Caenorhabditis elegans
by: Katsufumi Dejima, et al.
Published: (2018-01-01) -
MDM2-BCL-XL PROTACs enable degradation of BCL-XL and stabilization of p53
by: Mengyang Chang, et al.
Published: (2022-08-01) -
Reversible Germline Dynamics of Caenorhabditis elegans During Exposure to Pathogenic Bacteria
by: Bollen, Daniel Paul
Published: (2023)