Drosophila TFIID binds to a conserved downstream basal promoter element that is present in many TATA-box-deficient promoters.

We describe the identification and characterization of a conserved downstream basal promoter element that is present in a subset of Drosophila TATA-box-deficient (TATA-less) promoters by using purified, epitope-tagged TFIID complex (eTFIID) from embryos of transgenic Drosophila. DNase I footprinting of the binding of eTFIID to TATA-less promoters revealed that the factor protected a region that extended from the initiation site sequence (about +1) to approximately 35 nucleotides downstream of the RNA start site. In contrast, there was no apparent upstream DNase I protection or hypersensitivity induced by eTFIID in the -25 to -30 region at which TATA motifs are typically located. Further studies revealed a conserved sequence motif, (A/G)G(A/T)CGTG, termed the downstream promoter element (DPE), which is located approximately 30 nucleotides downstream of the RNA start site of many TATA-less promoters. DNase I footprinting and in vitro transcription experiments revealed that a DPE in its normal downstream location is necessary for transcription of DPE-containing TATA-less promoters and can compensate for the disruption of an upstream TATA box of a TATA-containing promoter. Moreover, a systematic mutational analysis of DNA sequences that encompass the DPE confirmed the importance of the consensus DPE sequence motif for basal transcription and further supports the postulate that the DPE is a distinct, downstream basal promoter element. These results suggest that the DPE acts in conjunction with the initiation site sequence to provide a binding site for TFIID in the absence of a TATA box to mediate transcription of TATA-less promoters.

[1]  M. Horikoshi,et al.  Identification of TFIID components required for transcriptional activation by upstream stimulatory factor. , 1993, The Journal of biological chemistry.

[2]  R. Kornberg,et al.  Identification and characterization of a TFIID-like multiprotein complex from Saccharomyces cerevisiae. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[3]  Kathryn S. Prickett,et al.  A Short Polypeptide Marker Sequence Useful for Recombinant Protein Identification and Purification , 1988, Bio/Technology.

[4]  D. Reinberg,et al.  Factors involved in specific transcription by mammalian RNA polymerase II: role of transcription factors IIA, IID, and IIB during formation of a transcription-competent complex , 1990, Molecular and cellular biology.

[5]  V. Corces,et al.  Expression of an activated ras gene causes developmental abnormalities in transgenic Drosophila melanogaster. , 1988, Genes & development.

[6]  D. Gilmour,et al.  Protein/DNA crosslinking of a TFIID complex reveals novel interactions downstream of the transcription start. , 1994, Nucleic acids research.

[7]  L. M. Lira,et al.  Sequence-specific transcriptional antirepression of the Drosophila Krüppel gene by the GAGA factor. , 1991, The Journal of biological chemistry.

[8]  M. Horikoshi,et al.  Drosophila 230-kD TFIID subunit, a functional homolog of the human cell cycle gene product, negatively regulates DNA binding of the TATA box-binding subunit of TFIID. , 1993, Genes & development.

[9]  R. Roeder,et al.  Interaction of a gene-specific transcription factor with the adenovirus major late promoter upstream of the TATA box region , 1985, Cell.

[10]  R. Tjian,et al.  Functional domains and upstream activation properties of cloned human TATA binding protein. , 1990, Science.

[11]  Young-Sun Lin,et al.  GAL4 derivatives function alone and synergistically with mammalian activators in vitro , 1988, Cell.

[12]  K. O'hare,et al.  Structure and transcription of the singed locus of Drosophila melanogaster. , 1991, Genetics.

[13]  D. Hogness,et al.  The Drosophila 74EF early puff contains E74, a complex ecdysone-inducible gene that encodes two ets-related proteins , 1990, Cell.

[14]  D. Hogness,et al.  The E75 ecdysone-inducible gene responsible for the 75B early puff in Drosophila encodes two new members of the steroid receptor superfamily. , 1990, Genes & development.

[15]  R. Tjian,et al.  Assembly of recombinant TFIID reveals differential coactivator requirements for distinct transcriptional activators , 1994, Cell.

[16]  S. Smale,et al.  Mechanism of initiator-mediated transcription: evidence for a functional interaction between the TATA-binding protein and DNA in the absence of a specific recognition sequence. , 1993, Molecular and cellular biology.

[17]  R. Young,et al.  The RNA polymerase II holoenzyme and its implications for gene regulation. , 1995, Trends in biochemical sciences.

[18]  P. Chambon,et al.  Cloning of the gene encoding the yeast protein BTF1Y, which can substitute for the human TATA box-binding factor. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[19]  P. Emanuel,et al.  TFIID sequence recognition of the initiator and sequences farther downstream in Drosophila class II genes. , 1994, Genes & development.

[20]  Robert Tjian,et al.  Isolation and characterization of the Drosophila gene encoding the TATA box binding protein, TFIID , 1990, Cell.

[21]  D. Ish-Horowicz,et al.  Functional analysis of the transcriptional control regions of the copia transposable element , 1986, The EMBO journal.

[22]  M. Delorenzi,et al.  Evidence that the Abdominal‐B r element function is conferred by a trans‐regulatory homeoprotein. , 1988, The EMBO journal.

[23]  M. Kozak Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes , 1986, Cell.

[24]  C. Kao,et al.  Yeast TATA-box transcription factor gene. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[25]  P. Sharp,et al.  Five intermediate complexes in transcription initiation by RNA polymerase II , 1989, Cell.

[26]  G. Rubin,et al.  Genetic transformation of Drosophila with transposable element vectors. , 1982, Science.

[27]  M. Meselson,et al.  Drosophila retrotransposon promoter includes an essential sequence at the initiation site and requires a downstream sequence for full activity. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[28]  I. Dawid,et al.  A family of oligo-adenylate-terminated transposable sequences in Drosophila melanogaster. , 1983, Journal of molecular biology.

[29]  P. Sharp,et al.  Function of a yeast TATA element-binding protein in a mammalian transcription system , 1988, Nature.

[30]  A. Hoffmann,et al.  Unique TATA‐binding protein‐containing complexes and cofactors involved in transcription by RNA polymerases II and III. , 1993, The EMBO journal.

[31]  Jun Ma,et al.  GAL4-VP16 is an unusually potent transcriptional activator , 1988, Nature.

[32]  I. Arkhipova,et al.  Properties of promoter regions of mdg1 Drosophila retrotransposon indicate that it belongs to a specific class of promoters. , 1991, The EMBO journal.

[33]  S. Smale,et al.  DNA sequence requirements for transcriptional initiator activity in mammalian cells. , 1994, Molecular and cellular biology.

[34]  V. Pirrotta Vectors for P-mediated transformation in Drosophila. , 1988, Biotechnology.

[35]  J. T. Kadonaga Assembly and disassembly of the Drosophila RNA polymerase II complex during transcription. , 1990, The Journal of biological chemistry.

[36]  Y. Ilyin,et al.  jockey, a mobile drosophila element similar to mammalian LINEs, is transcribed from the internal promoter by RNA polymerase II , 1988, Cell.

[37]  J. T. Kadonaga,et al.  A spectrum of mechanisms for the assembly of the RNA polymerase II transcription preinitiation complex , 1995, Molecular and cellular biology.

[38]  J. T. Kadonaga,et al.  Fractionation of the general RNA polymerase II transcription factors from Drosophila embryos. , 1990, The Journal of biological chemistry.

[39]  A. Mazo,et al.  Evidence for horizontal transmission of the mobile element jockey between distant Drosophila species. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[40]  R. Tjian,et al.  Diverse transcriptional functions of the multisubunit eukaryotic TFIID complex. , 1992, The Journal of biological chemistry.

[41]  M. Horikoshi,et al.  Molecular cloning, expression, and characterization of the Drosophila 85-kilodalton TFIID subunit , 1993, Molecular and cellular biology.

[42]  K. Livak Detailed structure of the Drosophila melanogaster stellate genes and their transcripts. , 1990, Genetics.

[43]  D. Reinberg,et al.  Common themes in assembly and function of eukaryotic transcription complexes. , 1995, Annual review of biochemistry.

[44]  S. Buratowski,et al.  The basics of basal transcription by RNA polymerase II , 1994, Cell.

[45]  D. Reinberg,et al.  News on initiation and elongation of transcription by RNA polymerase II. , 1995, Current opinion in cell biology.

[46]  K. Saigo,et al.  Structural variations in the Drosophila retrotransposon, 17.6. , 1986, Nucleic acids research.

[47]  G M Rubin,et al.  DNA sequence of the white locus of Drosophila melanogaster. , 1984, Journal of molecular biology.

[48]  C. Thummel The Drosophila E74 promoter contains essential sequences downstream from the start site of transcription. , 1989, Genes & development.

[49]  R. Tjian,et al.  Molecular cloning and functional analysis of Drosophila TAF110 reveal properties expected of coactivators , 1993, Cell.

[50]  Qiang Zhou,et al.  Holo-TFIID supports transcriptional stimulation by diverse activators and from a TATA-less promoter. , 1992, Genes & development.

[51]  W. Gehring,et al.  Molecular analysis of the dominant homeotic Antennapedia phenotype , 1987, The EMBO journal.

[52]  R. Tjian,et al.  Drosophila TFIIA-L is processed into two subunits that are associated with the TBP/TAF complex. , 1993, Genes & development.

[53]  D. Hultmark,et al.  Translational and transcriptional control elements in the untranslated leader of the heat-shock gene hsp22 , 1986, Cell.