Abstract

Mediator complex is essential for transcription by RNA polymerase II in eukaryotes. Although chromatin remodeling is an integral part of transcriptional activation at many promoters, whether Mediator is required for this function has not been determined. Here we have used the yeast CHA1 gene to study the role of Mediator in chromatin remodeling and recruitment of the transcription machinery. We show by chromatin immunoprecipitation that Mediator subunits are recruited to the induced CHA1 promoter. Inactivation of Mediator at 37 degrees C in yeast harboring the srb4-138 (med17) ts mutation severely reduces CHA1 activation and prevents recruitment to the induced CHA1 promoter of Med18/Srb5, from the head module of Mediator, and Med14/Rgr1, which bridges the middle and tail modules. In contrast, recruitment of Med15/Gal11 from the tail module is unaffected in med17 ts yeast at 37 degrees C. Recruitment of TATA-binding protein (TBP) is severely compromised in the absence of functional Mediator, whereas Kin28 and polymerase II recruitment are reduced but to a lesser extent. Induced levels of histone H3K4me3 at the CHA1 promoter are not diminished by inactivation of Mediator, whereas recruitment of Paf1 and of Ser2- and Ser5-phosphorylated forms of Rbp1 are reduced but not eliminated. Loss of histone H3 from the induced CHA1 promoter is seen in wild type yeast but is greatly reduced by loss of intact Mediator. In contrast, Swi/Snf recruitment and nucleosome remodeling are unaffected by loss of Mediator function. Thus, Mediator is required for recruitment of the transcription machinery subsequent to chromatin remodeling during CHA1 induction.

Highlights

  • The Mediator complex functions as an intermediary between activators and the general transcriptional machinery in eukaryotes, and its importance in messenger RNA transcription has been demonstrated both for individual genes and genomewide (1–5)

  • It was shown that such direct recruitment of Mediator was accompanied by Swi/Snf recruitment and that recruitment of Swi/ Snf to the activated GAL1 promoter depends on functional Mediator complex (34)

  • Ref. 1 Ref. 1 This study This study This study This study This study This study This study This study This study This study This study This study This study This study This study This study This study. To address this issue and to further our understanding of the role of the Mediator complex in gene activation, we have investigated the induction of the S. cerevisiae CHA1 gene

Read more

Summary

EXPERIMENTAL PROCEDURES

Yeast Strains and Growth—Yeast cultures were grown on complete synthetic dropout media. Yeast cultures were rapidly shifted to 37 °C by adding an equal volume of medium prewarmed to 50 °C to cultures grown at 25 °C. Strains RMY511 and RMY512 were derived from H3028 (47). Strains RMY521 and RMY522 were derived from MSY120 (48). Strains RMY541 and RMY542 were derived from HQY389 (49). Strains RMY551 and RMY552 were derived from BY4741 using EcoRV-digested pHQ1300 (a generous gift of Hongfang Qiu and Alan Hinnebusch) to introduce a 10ϫ Myc tag to Rpb prior to replacement of the endogenous SRB4 with plasmid-borne SRB4 or srb138. Strains RMY513-516, RMY531, RMY532, RMY561, and RMY562 were derived from the yeast TAP-tagged collection (50). Chromatin Immunoprecipitation (ChIP)—ChIP was performed essentially as described, except that cross-linking was done at 37 °C and with the following modifications (40, 51, 52). A washing, ECL (GE Healthcare) was used to illuminate the reactive band

RESULTS
K4 trimethylation
DISCUSSION
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.