Screening and Identification of NsylCBL Family Members Interacting with Protein Kinase NsylCIPK24a in Nicotiana Sylvestris

Author(s):  
Lulu An ◽  
Jingjing Mao ◽  
Haoyu Che ◽  
Sujuan Shi ◽  
Lianhong Dong ◽  
...  
1994 ◽  
Vol 269 (51) ◽  
pp. 32358-32367
Author(s):  
A Toker ◽  
M Meyer ◽  
K K Reddy ◽  
J R Falck ◽  
R Aneja ◽  
...  

2003 ◽  
Vol 279 (2) ◽  
pp. 1392-1399 ◽  
Author(s):  
Antonio E. Rusiñol ◽  
Douglas Thewke ◽  
June Liu ◽  
Natalie Freeman ◽  
Sankhavaram R. Panini ◽  
...  

Author(s):  
D. J. Burns ◽  
P. V. Basta ◽  
W. D. Holmes ◽  
L. M. Ballas ◽  
N. B. Rankl ◽  
...  

2001 ◽  
Vol 356 (2) ◽  
pp. 473-480 ◽  
Author(s):  
Kathryn M. SCHUBERT ◽  
Vincent DURONIO

Alterations in the expression of various Bcl-2 family members may act as one means by which a cell's survival may be regulated. The mechanism by which cytokines regulate expression of Bcl-2 family members was examined in the haemopoietic cell line TF-1. Cytokine-induced Mcl-1 protein expression was shown to be controlled through a pathway dependent upon phosphatidylinositol 3-kinase (PI 3-kinase). The cytokine-induced increase in mRNA transcription was not dependent upon PI 3-kinase, thus dissociating the immediate-early transcription factors responsible for Mcl-1 transcription from the PI 3-kinase signalling pathway. In contrast, Mcl-1 mRNA levels were dependent upon MEK [mitogen-activated protein kinase (MAPK)/extracellular-signal-regulated protein kinase kinase] activation, suggesting a role for the Ras/MEK/MAPK pathway in Mcl-1 transcription. Activation of PI 3-kinase was shown to be necessary to stimulate Mcl-1 protein translation. This was not due to any effect on prolonging the half-life of the protein. Finally, the lipid second messenger ceramide was shown to cause a reduction in Mcl-1 protein translation, probably via its ability to inhibit protein kinase B activation, providing further clues regarding the death-inducing effect of this lipid.


1992 ◽  
Vol 12 (9) ◽  
pp. 3930-3938 ◽  
Author(s):  
S Osada ◽  
K Mizuno ◽  
T C Saido ◽  
K Suzuki ◽  
T Kuroki ◽  
...  

A new protein kinase C (PKC)-related cDNA with unique tissue distribution has been isolated and characterized. This cDNA encodes a protein, nPKC theta, which consists of 707 amino acid residues and showed the highest sequence similarity to nPKC delta (67.0% in total). nPKC theta has a zinc-finger-like cysteine-rich sequence (C1 region) and a protein kinase domain sequence (C3 region), both of which are common in all PKC family members. However, nPKC theta lacks a putative Ca2+ binding region (C2 region) that is seen only in the conventional PKC subfamily (cPKC alpha, -beta I, -beta II, and -gamma) but not in the novel PKC subfamily (nPKC delta, -epsilon, -zeta, and -eta). Northern (RNA) blot analyses revealed that the mRNA for nPKC theta is expressed predominantly in skeletal muscle. Furthermore, nPKC theta mRNA is the most abundantly expressed PKC isoform in skeletal muscle among the nine PKC family members. nPKC theta expressed in COS1 cells serves as a phorbol ester receptor. By the use of an antipeptide antibody specific to the D2-D3 region of the nPKC theta sequence, nPKC theta was recognized as a 79-kDa protein upon sodium dodecyl sulfate-polyacrylamide gel electrophoresis in mouse skeletal muscle extract and also in an extract from COS1 cells transfected with an nPKC theta cDNA expression plasmid. Autophosphorylation of immunoprecipitated nPKC theta was observed; it was enhanced by phosphatidylserine and 12-O-tetradecanoylphorbol-13-acetate but attenuated by the addition of Ca2+. These results clearly demonstrate that nPKC theta should be considered a member of the PKC family of proteins that play crucial roles in the signal transduction pathway.


2011 ◽  
Vol 48 (12-13) ◽  
pp. 1484-1493 ◽  
Author(s):  
Jolyn Johnson ◽  
Céline Molle ◽  
Ezra Aksoy ◽  
Michel Goldman ◽  
Stanislas Goriely ◽  
...  

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