Expression, proteolytic analysis, reconstitution, and crystallization of the tau60/tau91 subcomplex of yeast TFIIIC.

Abstract:

:The transcription factor IIIC (TFIIIC) is a multisubunit DNA-binding factor required for promoter recognition and TFIIIB assembly on tRNA genes transcribed by RNA polymerase III. Yeast TFIIIC consists of six subunits, organized in the two globular subcomplexes tauA and tauB, which recognize two internal tDNA promoter elements, the A and the B block, respectively. As a first step toward a detailed structural analysis of TFIIIC, we report here the expression, proteolytic analysis, reconstitution, and crystallization of the complex between yeast TFIIIC subunits tau91 and tau60. Proteolysis provided an insight into the domain structure of tau60 and tau91. Both the proteins form a stable complex that does not require an N-terminal, protease-sensitive extension of tau91. Crystals diffracting beyond 3.2 A were obtained from a complex formed by full-length tau60 and the N-terminally truncated form of tau91 lacking this extension.

journal_name

Protein Expr Purif

authors

Mylona A,Acker J,Fernández-Tornero C,Sentenac A,Müller CW

doi

10.1016/j.pep.2005.06.013

keywords:

subject

Has Abstract

pub_date

2006-02-01 00:00:00

pages

255-61

issue

2

eissn

1046-5928

issn

1096-0279

pii

S1046-5928(05)00226-3

journal_volume

45

pub_type

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