Localization of the yeast RNA polymerase I-specific subunits

被引:41
作者
Bischler, N
Brino, L
Carles, C
Riva, M
Tschochner, H
Mallouh, V
Schultz, P
机构
[1] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, CU Strasbourg, France
[2] Ecole Super Biotechnol Strasbourg, Pole API, F-67400 Illkirch Graffenstaden, France
[3] CEA Saclay, Serv Biochim & Genet Mol, F-91191 Gif Sur Yvette, France
[4] Biochem Zentrum Heidelberg, D-69120 Heidelberg, Germany
关键词
atomic structure docking; cryo-electron microscopy; epitope localization; immunolabelling; yeast RNA polymerase I (A);
D O I
10.1093/emboj/cdf392
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The spatial distribution of four subunits specifically associated to the yeast DNA-dependent RNA polymerase I (RNA pol I) was studied by electron microscopy. A structural model of the native enzyme was determined by cryo-electron microscopy from isolated molecules and was compared with the atomic structure of RNA pol II Delta4/7, which lacks the specific polypeptides. The two models were aligned and a difference map revealed four additional protein densities present in RNA pol I, which were characterized by immunolabelling. A protruding protein density named stalk was found to contain the RNA pol I-specific subunits A43 and A14. The docking with the atomic structure showed that the stalk protruded from the structure at the same site as the C-terminal domain (CTD) of the largest subunit of RNA pol II. Subunit A49 was placed on top of the clamp whereas subunit A34.5 bound at the entrance of the DNA binding cleft, where it could contact the downstream DNA. The location of the RNA pol I-specific subunits is correlated with their biological activity.
引用
收藏
页码:4136 / 4144
页数:9
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