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Journal ArticleDOI

On a roll for new TRF targets

15 Nov 2007-Genes & Development (Cold Spring Harbor Laboratory)-Vol. 21, Iss: 22, pp 2855-2860
TL;DR: 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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Citations
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Journal ArticleDOI
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.

489 citations


Cites background from "On a roll for new TRF targets"

  • ...This concept is nicely exemplified in studies of the TBP-related factors (TRFs) (for reviews, see: Jones, 2007; Müller et al., 2007; Reina and Hernandez, 2007; Torres-Padilla and Tora, 2007)....

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Journal ArticleDOI
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.

380 citations

Journal ArticleDOI
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.

193 citations


Cites background from "On a roll for new TRF targets"

  • ...The other subunits of TFIID (the TBP-associated factors or TAFs) appear to interact with INR and DPEs....

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  • ...Leurent C, Sanders S, Ruhlmann C, Mallouh V, Weil PA, Kirschner DB, Tora L, Schultz P: Mapping histone fold TAFs within yeast TFIID....

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  • ...In higher eukaryotes, there are multiple genes encoding TBP-related factors (TRFs) and variant TAFs [1,7]....

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Journal ArticleDOI
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.

140 citations


Cites background from "On a roll for new TRF targets"

  • ...which is essential for interaction with the TATA box (reviewed in [121-123, 144-146]....

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

83 citations

References
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Journal ArticleDOI
TL;DR: It is suggested that, even if higher eukaryotes generally contain multiple tbp -related genes, TLP is not a bona fide mammalian counterpart of Drosophila TRF.
Abstract: TATA-binding protein (TBP) is an essential factor for eukaryotic transcription. In this study, we demonstrated a mouse cDNA encoding a 21 kDa TBP-like protein (TLP). The TLP ORF, carrying 186 amino acids, covered the entire 180 amino acids of the C-terminal conserved domain of mouse TBP with 39% identity and 76% similarity. Northern blot analysis demonstrated that TLP mRNAs were expressed in various mammalian tissues ubiquitously and that their distribution pattern was analogous to that of TBP. By using anti-TLP antibody, we demonstrated the existence of TLP proteins in various mammalian cells and tissues. The Drosophila TBP-related factor (TRF) is a neurogenesis-related transcription factor that binds to the TATA-box and activates transcription. TLP did not bind to the TATA-box nor direct transcription initiation. Multiple amino acids critical for TBP function were deleted or substituted in TLP, while amino acids in Drosophila TRF much resembled those in TBP. Similarity between Drosophila TRF and mouse TLP was considerably lower (alignment score 35) than that between Drosophila TBP and mouse TBP (alignment score 88). Identity of nucleotide sequences between mouse and putative human TLPs (94%) was higher than that between TBPs (91%) in these two animals. Expression of TLP was nearly constant throughout the P19 differentiation process. Accordingly, we suggest that, even if higher eukaryotes generally contain multiple tbp -related genes, TLP is not a bona fide mammalian counterpart of Drosophila TRF.

84 citations


"On a roll for new TRF targets" refers background or methods in this paper

  • ...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)....

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  • ...…was discovered by analysis of ESTs by several groups and, accordingly, variously named TRF2 (Rabenstein et al. 1999; Teichmann et al. 1999), TRF (Maldonado 1999), TLP (Ohbayashi et al. 1999, 2001), TLF (Kaltenbach et al. 2000; Veenstra et al. 2000), or TBPrelated protein (TRP) (Moore et al. 1999)....

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  • ...TRF2 was discovered by analysis of ESTs by several groups and, accordingly, variously named TRF2 (Rabenstein et al. 1999; Teichmann et al. 1999), TRF (Maldonado 1999), TLP (Ohbayashi et al. 1999, 2001), TLF (Kaltenbach et al. 2000; Veenstra et al. 2000), or TBPrelated protein (TRP) (Moore et al. 1999)....

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Journal ArticleDOI
29 Sep 2000-Cell
TL;DR: It is shown that TLF is an essential transcription factor required for transcription of a restricted set of specific genes in the early C. elegans embryo and a number of significant questions arise.

79 citations


"On a roll for new TRF targets" refers background in this paper

  • ...%) between TRF2 and TBP core domains suggests that they adopt the same saddle-like structure, the TBP residues required for TATA-box binding are not conserved in TRF2, suggesting that TRF2 requires other elements to bind DNA (see Berk 2000 and references therein)....

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  • ...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)....

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Journal ArticleDOI
TL;DR: The discovery of TBP-related factors in many metazoan organisms and a mammalian complex that can mediate RNA polymerase II transcription independently of T BP in vitro suggest that TBP might not have such a universal role as previously imagined.

74 citations


"On a roll for new TRF targets" refers background in this paper

  • ...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)....

    [...]

Journal ArticleDOI
TL;DR: It is demonstrated that the Drosophila TATA box-binding protein (TBP)-related factor 2 (TRF2 or TLF) encodes two protein isoforms: the previously described 75-kDa TRF2 and a newly identified 175- kDa version in which the same sequence is preceded by a long N-terminal domain with coiled-coil motifs.
Abstract: The Drosophila TATA box-binding protein (TBP)-related factor 2 (TRF2 or TLF) was shown to control a subset of genes different from that controlled by TBP. Here, we have investigated the structure and functions of the trf2 gene. We demonstrate that it encodes two protein isoforms: the previously described 75-kDa TRF2 and a newly identified 175-kDa version in which the same sequence is preceded by a long N-terminal domain with coiled-coil motifs. Chromatography of Drosophila embryo extracts revealed that the long TRF2 is part of a multiprotein complex also containing ISWI. Both TRF2 forms are detected at the same sites on polytene chromosomes and have the same expression patterns, suggesting that they fulfill similar functions. A study of the manifestations of the trf2 mutation suggests an essential role of TRF2 during embryonic Drosophila development. The trf2 gene is strongly expressed in germ line cells of adult flies. High levels of TRF2 are found in nuclei of primary spermatocytes and trophocytes with intense transcription. In ovaries, TRF2 is present both in actively transcribing nurse cells and in the transcriptionally inactive oocyte nuclei. Moreover, TRF2 is essential for premeiotic chromatin condensation and proper differentiation of germ cells of both sexes.

53 citations


"On a roll for new TRF targets" refers background or result in this paper

  • ...…by TRF2 rather than TBP. Consistent with a broad role of TRF2, TRF2-deficient flies are not viable, and partial TRF2 inactivation leads to various defects such as impaired premeiotic chromatin condensation and differentiation of male and female germ cells (Kopytova et al. 2006; Shima et al. 2007)....

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  • ...This provides a possible mechanism for earlier observations linking TRF2 with chromatin structure (Martianov et al. 2002; Kopytova et al. 2006)....

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  • ...This is consistent with studies in nematode, fly, fish, and frog, where inactivation of TRF2 results in a block in embryonic development and lethality (Dantonel et al. 2000; Kaltenbach et al. 2000; Veenstra et al. 2000; Bartfai et al. 2004; Kopytova et al. 2006)....

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  • ...…however, associate with TFIIA and TFIIB (Moore et al. 1999), and in fact is found complexed with TFIIA in a HeLa cell line expressing a tagged TRF2, and with TFIIA-like factor (ALF), a TFIIA paralog expressed in male germ cells (Teichmann et al. 1999; Catena et al. 2005; Kopytova et al. 2006)....

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Journal ArticleDOI
TL;DR: It is suggested that in Drosophila and possibly other insects the alternative TRF1/BRF complex appears responsible for the initiation of all known classes of Pol III transcription.
Abstract: Metazoans have evolved multiple paralogues of the TATA binding protein (TBP), adding another tunable level of gene control at core promoters. While TBP-related factor 1 (TRF1) shares extensive homology with TBP and can direct both Pol II and Pol III transcription in vitro, TRF1 target sites in vivo have remained elusive. Here, we report the genome-wide identification of TRF1-binding sites using high-resolution genome tiling microarrays. We found 354 TRF1-binding sites genome-wide with ∼78% of these sites displaying colocalization with BRF. Strikingly, the majority of TRF1 target genes are Pol III-dependent small noncoding RNAs such as tRNAs and small nonmessenger RNAs. We provide direct evidence that the TRF1/BRF complex is functionally required for the activity of two novel TRF1 targets (7SL RNA and small nucleolar RNAs). Our studies suggest that unlike most other eukaryotic organisms that rely on TBP for Pol III transcription, in Drosophila and possibly other insects the alternative TRF1/BRF complex appears responsible for the initiation of all known classes of Pol III transcription.

48 citations