Detailed Information on Publication Record
2005
Interaction between Rtg2p and Mks1p in the regulation of the RTG pathway of Saccharomyces cerevisiae.
ŠPÍREK, Mário, JR FERREIRA JÚNIOR and Ronald BUTOWBasic information
Original name
Interaction between Rtg2p and Mks1p in the regulation of the RTG pathway of Saccharomyces cerevisiae.
Name in Czech
Interakce mezi Rtg2p a Mks1p v regulaci RTG dráhy Saccharomyces cerevisiae
Authors
ŠPÍREK, Mário (703 Slovakia, guarantor), JR FERREIRA JÚNIOR (76 Brazil) and Ronald BUTOW (840 United States of America)
Edition
Gene, Elsevier, 2005, 0378-1119
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10600 1.6 Biological sciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.694
RIV identification code
RIV/00216224:14310/05:00035909
Organization unit
Faculty of Science
UT WoS
000231497200002
Keywords (in Czech)
retrogradni regulace, RTG dráha, Rtg2, Mks1, kvasinka
Keywords in English
Retrograde regulation; RTG pathway; Rtg2p; Mks1p; Yeast
Tags
Tags
International impact, Reviewed
Změněno: 23/6/2009 12:26, RNDr. Mário Špírek, PhD.
V originále
Retrograde signaling mediates nuclear gene expression in response to changes in the functional state of mitochondria. In budding yeast, retrograde signaling, also termed the RTG pathway, relies on the heterodimeric, basic helix-loop-helix zipper transcription factors, Rtg1p and Rtg3p, for the activation of target gene expression. Activation of the RTG pathway leads to partial dephosphorylation of Rtg3p and its translocation, together with Rtg1p, from the cytoplasm to the nucleus. These processes depend on a positive regulatory factor, Rtg2p, a novel protein with a ATP binding domain similar to that of the Hsp70/actin/sugar kinase superfamily. Four negative regulatory factors, Lst8p, Mks1p, and two redundant 14-3-3 proteins, Bmh1/2p, function between Rtg2p and Rtg1/3p. Alternative interaction between Mks1p and Rtg2p or Bmh1/2p provides a means for regulation of the RTG pathway. When the RTG pathway is on, Mks1p is inactivated by its association with Rtg2p; and when the RTG pathway is off, Mks1p dissociates from Rtg2p and forms a complex with Bmh1/2p, which is the negative regulatory form of Mks1p. Here we show that Rtg2p and Mks1p can interact in the absence of other factors, and is thereby the minimal binary switch for regulation of the RTG pathway. Gel filtration experiments indicate that both Rtg2p and Mks1p exist in high molecular weight complexes. In response to changes in the activity of the RTG pathway, both Rtg2p and Mks1p shift to different sized high molecular weight complexes. Together, our data suggest that dynamic association between Mks1p and Rtg2p in high molecular weight complexes provides a means to regulate the RTG pathway.
In Czech
Experimenty využívajíc gelovou filtraci naznačili, že Mks1 i Rtg2 existují ve vysoko molekulárních komplexech. Velkost techto komplexú reaguje na aktivitu RTG dráhy.