Literature DB >> 1586947

The TATA-binding protein is required for transcription by all three nuclear RNA polymerases in yeast cells.

B P Cormack1, K Struhl.   

Abstract

Using temperature- and proteolytically sensitive derivatives to inactivate the function of the yeast TATA-binding protein (TBP) in vivo, we investigated the requirement of TBP for transcription by the three nuclear RNA polymerases in yeast cells. TBP is required for RNA polymerase II (pol II) transcription from promoters containing conventional TATA elements as well as functionally distinct promoters that lack TATA-like sequences. TBP is also required for transcription of the U6 snRNA and two different tRNA genes mediated by RNA pol III as well as transcription of ribosomal RNA mediated by RNA pol I. For all promoters tested, transcription decreases rapidly and specifically upon inactivation of TBP, strongly suggesting that TBP is directly involved in the transcription process. These observations suggest that TBP is required for transcription of all nuclearly encoded genes in yeast, although distinct molecular mechanisms are probably involved for the three RNA polymerase transcription machineries.

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Year:  1992        PMID: 1586947     DOI: 10.1016/0092-8674(92)90232-2

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  167 in total

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5.  New model for the yeast RNA polymerase I transcription cycle.

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7.  Loss of the Rpb4/Rpb7 subcomplex in a mutant form of the Rpb6 subunit shared by RNA polymerases I, II, and III.

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8.  Identification of regulatory elements within the minimal promoter region of the human endogenous ERV9 proviruses: accurate transcription initiation is controlled by an Inr-like element.

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10.  RPD3 is required for the inactivation of yeast ribosomal DNA genes in stationary phase.

Authors:  Joseph J Sandmeier; Sarah French; Yvonne Osheim; Wang L Cheung; Christopher M Gallo; Ann L Beyer; Jeffrey S Smith
Journal:  EMBO J       Date:  2002-09-16       Impact factor: 11.598

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