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Open AccessJournal ArticleDOI

On a roll for new TRF targets

Jaime H. Reina, +1 more
- 15 Nov 2007 - 
- Vol. 21, Iss: 22, pp 2855-2860
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TLDR
In this issue of Genes & Development, Isogai et al. (2007a) report that the TATA-less histone H1 promoter is regulated by TRF2, which provides a possible mechanism for earlier observations linking TRF3 with chromatin structure and helps to establish Drosophila TRF 2 as a broadly used core-promoter factor.
Abstract
In the early 1990s, one of us wrote in these pages a review entitled “TBP, a universal transcription factor?” (Hernandez 1993). At the time, it had become clear that the TATA-box-binding protein TBP was not a transcription factor exclusively involved in transcription from RNA polymerase II (pol II) promoters as had been thought before, but rather a factor involved in transcription by all three main types of eukaryotic nuclear RNA polymerases. In retrospect, however, the question mark at the end of the title was a wise touch! Indeed, shortly thereafter, the first TBP-related factor, TRF1, was described (Crowley et al. 1993). Since then, two more TRFs have been discovered (for review, see Berk 2000; Davidson 2003; Hochheimer and Tjian 2003), and it was found that some genes dispense with TBP and TRFs altogether (Wieczorek et al. 1998). This “expansion” of TBP into a TBP family of proteins begs the question of which promoters are targeted by which TBP family member. In this issue of Genes & Development, Isogai et al. (2007a) report that the TATA-less histone H1 promoter is regulated by TRF2. This provides a possible mechanism for earlier observations linking TRF2 with chromatin structure (Martianov et al. 2002; Kopytova et al. 2006). Furthermore, the identification by Isogai et al. (2007a) of a large number of TRF2-bound sites in the Drosophila genome helps to establish Drosophila TRF2 as a broadly used core-promoter factor. Among the three classes of TBP-related factors described so far, TRF2—also called TBP-like protein (TLP) or TBP-like factor (TLF)—is the only one to be widely present in metazoans (Ohbayashi et al. 1999; Kaltenbach et al. 2000; Veenstra et al. 2000). TRF1 has been found only in Drosophila and Anopheles (Crowley et al. 1993; Isogai et al. 2007b), and TRF3 is restricted to vertebrates (Persengiev et al. 2003). All three proteins contain a core domain related to the TBP C-terminal core domain, and some also contain variable Nand C-terminal domains.

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Journal ArticleDOI

Regulation of gene expression via the core promoter and the basal transcriptional machinery.

TL;DR: The findings suggest that the core promoter and basal transcription factors are important yet mostly unexplored components in the regulation of gene expression.
Journal ArticleDOI

The RNA Polymerase II Core Promoter – the Gateway to Transcription

TL;DR: The core promoter is a sophisticated gateway to transcription that determines which signals will lead to transcription initiation and may contain many different sequence motifs that specify different mechanisms of transcription and responses to enhancers.
Journal ArticleDOI

The basal initiation machinery: beyond the general transcription factors.

TL;DR: A simple model in which basal transcription factors sequentially assembled with RNA Polymerase II to generate a preinitiation complex (PIC) indicates that PIC composition is not universal, but promoter-dependent.
Journal ArticleDOI

The core promoter: At the heart of gene expression.

TL;DR: A broad spectrum of studies that highlight the importance of the core promoter and its pivotal role in the regulation of metazoan gene expression are reviewed and future research directions and challenges are suggested.
Journal ArticleDOI

Developmental regulation of transcription initiation: more than just changing the actors.

TL;DR: The proposed models of transcription initiation by alternative initiation complexes in distinct stages of developmental specialization during vertebrate ontogeny are summarized.
References
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Journal ArticleDOI

Spermiogenesis Deficiency in Mice Lacking the Trf2 Gene

TL;DR: It is speculated that mammals may have evolved more specialized TRF2 functions in the testis that involve transcriptional regulation of genes essential for spermiogenesis.
Journal ArticleDOI

TATA Box-Binding Protein (TBP)-Related Factor 2 (TRF2), a Third Member of the TBP Family

TL;DR: The cloning of a TBP-related factor (TRF2) that is found in humans, Drosophila, Caenorhabditis elegans, and other metazoans is reported, suggesting that meetazoans have evolved multiple TBPs to accommodate the vast increase in genes and expression patterns during development and cellular differentiation.
Journal ArticleDOI

Transcription properties of a cell type-specific TATA-binding protein, TRF.

TL;DR: Findings suggest TRF is a homolog of TBP that functions to direct tissue- and gene-specific transcription in vitro, and forms a stable complex containing multiple novel subunits, nTAFs.
Journal ArticleDOI

Novel 8-base pair sequence (Drosophila DNA replication-related element) and specific binding factor involved in the expression of Drosophila genes for DNA polymerase alpha and proliferating cell nuclear antigen.

TL;DR: Evidence is obtained for a protein factor (DREF) in the nuclear extract of cultured Drosophila cells (Kc cells), and this factor specifically binds to DREs of both genes, and it is concluded that DREF is associated with the 86-kDa polypeptide.
Journal ArticleDOI

Switching of the core transcription machinery during myogenesis

TL;DR: It is reported that differentiation of myoblast to myotubes involves the disruption of the canonical holo-TFIID and replacement by a novel TRF3/TAF3 (TBP-related factor 3/TATA-binding protein-associated factor 3) complex, which provides organisms a simple yet effective means to selectively turn on one transcriptional program while silencing many others.
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