TY - JOUR
T1 - The structural and functional role of Med5 in the yeast mediator tail module
AU - Hu, Guo-Zhen
AU - Ronne, Hans
AU - Béve, Jenny
AU - Myers, Lawrence
AU - Werngren, Olivera
AU - Gustafsson, Claes
AU - Hultenby, Kjell
AU - Wibom, Rolf
AU - Balciunas, Darius
AU - Balciunas, Darius
PY - 2005
Y1 - 2005
N2 - Med5 (Nut1) is identified here as a component of the Mediator tail region. Med5 is positioned peripherally to Med16 (Sin4) together with the three members of the putative Gal11 module, Med15 (Gal11), Med2, and Med3 (Pgd1). The biochemical analysis receives support from genetic interactions between med5 Delta and med15 Delta deletions. The med5 Delta and med16 Delta deletion strains share many phenotypes, including effects on mitochondrial function with enhanced growth on nonfermentable carbon sources, increased citrate synthase activity, and increased oxygen consumption. Deletion of the MED5 gene leads to increased transcription of nuclear genes encoding components of the oxidative phosphorylation machinery, whereas mitochondrial genes encoding components of the same machinery are down-regulated. We discuss a possible role for Med5 in coordinating nuclear and mitochondrial gene transcription.
AB - Med5 (Nut1) is identified here as a component of the Mediator tail region. Med5 is positioned peripherally to Med16 (Sin4) together with the three members of the putative Gal11 module, Med15 (Gal11), Med2, and Med3 (Pgd1). The biochemical analysis receives support from genetic interactions between med5 Delta and med15 Delta deletions. The med5 Delta and med16 Delta deletion strains share many phenotypes, including effects on mitochondrial function with enhanced growth on nonfermentable carbon sources, increased citrate synthase activity, and increased oxygen consumption. Deletion of the MED5 gene leads to increased transcription of nuclear genes encoding components of the oxidative phosphorylation machinery, whereas mitochondrial genes encoding components of the same machinery are down-regulated. We discuss a possible role for Med5 in coordinating nuclear and mitochondrial gene transcription.
UR - https://res.slu.se/id/publ/7558
UR - http://www.jbc.org/cgi/content/full/280/50/41366
U2 - 10.1074/jbc.M511181200
DO - 10.1074/jbc.M511181200
M3 - Journal article
C2 - 16230344
SN - 0021-9258
VL - 280
SP - 41366
EP - 41372
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 50
ER -