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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

TBP2 is a substitute for TBP in Xenopus oocyte transcription

TL;DR: TBP2 is the predominant initiation factor in oocytes, which is substituted by TBP on a subset of promoters in embryos as a result of proteolytic degradation of TBP2 during meiotic maturation, suggesting a redundant role in this repression or a role in initiation factor switching between oocytes and embryos.
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Cleavage of TFIIA by Taspase1 Activates TRF2-Specified Mammalian Male Germ Cell Programs

TL;DR: This study presents a paradigm in which a protease (Taspase1) cleaves a ubiquitously expressed GTF (TFIIA) to enable tissue-specific (testis) transcription, meeting the demand for sophisticated regulation of distinct subsets of genes in higher organisms.
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Message in a nucleus: signaling to the transcriptional machinery

TL;DR: This work discusses three mechanisms through which signaling pathways can interact with complexes that alter chromatin structure or recruit RNA polymerase II, and suggests that individual regulatory proteins may integrate a variety of signals, allowing crosstalk between pathways.
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General transcription factors and subunits of RNA polymerase III: Paralogs for promoter- and cell type-specific transcription in multicellular eukaryotes.

TL;DR: Paralogs of transcription factors and of the RPC32 subunit of RNA polymerase III play important roles in cell type- and promoter-specific transcription in multi-cellular eukaryotes.
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TRF2: TRansForming the view of general transcription factors.

TL;DR: This work reviews the recent findings implicating TRF2 as a basal transcription factor in the regulation of diverse biological processes and specialized transcriptional programs and examines its role in TATA box binding and core promoter elements.
References
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Systematic determination of patterns of gene expression during Drosophila embryogenesis

TL;DR: Analyzing gene-expression patterns by in situ hybridization to whole-mount embryos provides an extremely rich dataset that can be used to identify genes involved in developmental processes that have been missed by traditional genetic analysis.
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Recruitment of RNA polymerase III to its target promoters

TL;DR: A key step in retrieving the information stored in the complex genomes of eukaryotes involves the identification of transcription units and, more specifically, the recognition of promoter sequences by RNA polymerase.
Journal ArticleDOI

Histone H1 Depletion in Mammals Alters Global Chromatin Structure but Causes Specific Changes in Gene Regulation

TL;DR: Results indicate that linker histones can participate in epigenetic regulation of gene expression by contributing to the maintenance or establishment of specific DNA methylation patterns.
Journal ArticleDOI

The regulation of histone synthesis in the cell cycle

TL;DR: The author’s views are based on personal experience, research, and interviews conducted at the 2016 USGS workshop on “Biology of infectious disease: Foundations of Natural Selection and Response to infectious disease .”
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