NDLI: Requirement for acidic amino acid residues immediately N-terminal to the conserved domain of Saccharomyces cerevisiae TFIID.

Please wait, while we are loading the content...

Year: 2016, Volume: 35

Year: 2015, Volume: 34

Year: 2014, Volume: 33

Year: 2013, Volume: 33

Year: 2013, Volume: 32

Year: 2012, Volume: 32

Year: 2012, Volume: 31

Year: 2011, Volume: 30

Year: 2010, Volume: 29

Year: 2009, Volume: 28

Year: 2008, Volume: 27

Year: 2007, Volume: 26

Year: 2006, Volume: 26

Year: 2006, Volume: 25

Year: 2005, Volume: 24

Year: 2004, Volume: 24

Year: 2004, Volume: 23

Year: 2003, Volume: 22

Year: 2002, Volume: 21

Year: 2001, Volume: 20

Year: 2000, Volume: 19

Year: 1999, Volume: 18

Year: 1998, Volume: 17

Year: 1997, Volume: 16

Year: 1996, Volume: 15

Year: 1995, Volume: 14

Year: 1994, Volume: 13

Year: 1993, Volume: 12

Year: 1992, Volume: 11

Year: 1991, Volume: 10

Year: 1991, Volume: 10, Issue: 13

Year: 1991, Volume: 10, Issue: 12

Year: 1991, Volume: 10, Issue: 11

Year: 1991, Volume: 10, Issue: 10

Year: 1991, Volume: 10, Issue: 9

Year: 1991, Volume: 10, Issue: 8

Year: 1991, Volume: 10, Issue: 7

Crystal structure of Penicillium citrinum P1 nuclease at 2.8 A resolution.

Site directed mutagenesis of the heme axial ligands of cytochrome b559 affects the stability of the photosystem II complex.

Cloning and in vivo expression of the human GART gene using yeast artificial chromosomes.

Molecular cloning and expression of a cDNA encoding the secretin receptor.

Pairwise, cooperative and inhibitory interactions describe the assembly and probable structure of the T-cell antigen receptor.

Exposed epitopes on a Trypanosoma equiperdum variant surface glycoprotein altered by point mutations.

Purification and properties of sialoadhesin, a sialic acid-binding receptor of murine tissue macrophages.

Release of acetylcholine by Xenopus oocytes injected with mRNAs from cholinergic neurons.

The orphan receptor cDNA RDC7 encodes an A1 adenosine receptor.

Functional consequences of single amino acid substitutions in calmodulin-activated adenylate cyclase of Bordetella pertussis.

The SH2 and SH3 domains of pp60src direct stable association with tyrosine phosphorylated proteins p130 and p110.

The Saccharomyces cerevisiae STE14 gene encodes a methyltransferase that mediates C-terminal methylation of a-factor and RAS proteins.

A novel ATPase complex selectively accumulated upon heat shock is a major cellular component of thermophilic archaebacteria.

Manganese superoxide dismutase can reduce cellular damage mediated by oxygen radicals in transgenic plants.

Endocytosis and targeting of exogenous HIV-1 Tat protein.

vac2: a yeast mutant which distinguishes vacuole segregation from Golgi-to-vacuole protein targeting.

One of three transmembrane stretches is sufficient for the functioning of the SecE protein, a membrane component of the E. coli secretion machinery.

Cytosolic and mitochondrial surface factor-independent import of a synthetic peptide into mitochondria.

Exonic sequences are required for elicitor and light activation of a plant defense gene, but promoter sequences are sufficient for tissue specific expression.

Light-inducible and constitutively expressed DNA-binding proteins recognizing a plant promoter element with functional relevance in light responsiveness.

A novel class of plant proteins containing a homeodomain with a closely linked leucine zipper motif.

A tobacco bZip transcription activator (TAF-1) binds to a G-box-like motif conserved in plant genes.

Expression of a monocot LHCP promoter in transgenic rice.

A T-cell specific TCR delta DNA binding protein is a member of the human GATA family.

NF-kappa B contacts DNA by a heterodimer of the p50 and p65 subunit.

Inhibition of transcription factors belonging to the rel/NF-kappa B family by a transdominant negative mutant.

A pause site for RNA polymerase II is associated with termination of transcription.

Requirement for acidic amino acid residues immediately N-terminal to the conserved domain of Saccharomyces cerevisiae TFIID.

TFIID is required for in vitro transcription of the human U6 gene by RNA polymerase III.

In vivo detection of snRNP-rich organelles in the nuclei of mammalian cells.

Characterization of the hormone responsive element involved in the regulation of the progesterone receptor gene.

Amino-terminal leucine-rich repeats in gonadotropin receptors determine hormone selectivity.

Human erythroid 5-aminolevulinate synthase: promoter analysis and identification of an iron-responsive element in the mRNA.

Identification of a novel iron-responsive element in murine and human erythroid delta-aminolevulinic acid synthase mRNA.

Specific expression of the tobacco Tnt1 retrotransposon in protoplasts.

The origin of footprints of the Tc1 transposon of Caenorhabditis elegans.

An indicator gene for detection of germline retrotransposition in transgenic Drosophila demonstrates RNA-mediated transposition of the LINE I element.

Histone-DNA interactions and their modulation by phosphorylation of -Ser-Pro-X-Lys/Arg- motifs.

Single-stranded replication intermediates of ribosomal DNA replicons of pea.

Year: 1991, Volume: 10, Issue: 6

Year: 1991, Volume: 10, Issue: 5

Year: 1991, Volume: 10, Issue: 4

Year: 1991, Volume: 10, Issue: 3

Year: 1991, Volume: 10, Issue: 2

Year: 1991, Volume: 10, Issue: 1

Year: 1990, Volume: 9

Year: 1989, Volume: 8

Year: 1988, Volume: 7

Year: 1987, Volume: 6

Year: 1986, Volume: 5

Year: 1985, Volume: 4

Year: 1984, Volume: 3

Year: 1983, Volume: 2

Year: 1982, Volume: 1

Requirement for acidic amino acid residues immediately N-terminal to the conserved domain of Saccharomyces cerevisiae TFIID.

Content Provider	PubMed Central
Author	Zhou, Q. A. Schmidt, M. C. Berk, A. J.
Abstract	TFIID binds to TATA boxes and initiates the assembly of general transcription factors and pol II on promoters. TFIID proteins from various species consist of a highly conserved carboxy terminal domain and very divergent amino terminal domains. We investigated the function of the non-conserved amino terminal domain (residues 1-60) of Saccharomyces cerevisiae TFIID (YIID, 240 residues) by testing the ability of a series of YIID amino terminal deletion mutants to complement a YIID deficient yeast strain. Mutants with deletions up to amino acid 48 restored the YIID deficient yeast strain to an apparently wild type phenotype. However, deletion up to position 57 or 60 produced yeast strains which formed extremely small colonies. Moreover, overexpression of YIID delta 2-57 or YIID delta 3-60 protein in the presence of wild type YIID resulted in a dominant-negative inhibition of growth. No difference between the basal transcriptional activity of wild type YIID and these amino terminal deletion mutants was observed in vitro. However, transcriptional activation in vivo of promoter-lacZ fusions showed that the YIID delta 2-57 deletion affects the ability of certain promoters (CUP1 and an HSP UAS-CYC1 promoter hybrid promoter) to respond to upstream factor stimulation. At least one inducible promoter, PHO5, was not affected by this deletion. The defect produced by YIID delta 2-57 was due to the deletion of several acidic residues present between residues 48 and 57. The results show that the conserved carboxy terminal domain of YIID is sufficient for cell viability. However, an acidic region just amino terminal to the conserved domain is required for normal growth and transcription control in most yeast strains.
Starting Page	1843
File Format	PDF
ISSN	14602075
e-ISSN	14602075
Journal	The EMBO Journal
Issue Number	7
Volume Number	10
Language	English
Publisher Date	1991-07-01
Access Restriction	Open
Subject Keyword	Research in Higher Education
Content Type	Text
Resource Type	Article
Subject	Neuroscience Immunology and Microbiology Medicine Molecular Biology

Central Library (ISO-9001:2015 Certified)
Indian Institute of Technology Kharagpur
Kharagpur, West Bengal, India | PIN - 721302

See location in the Map
03222 282435
Mail: support@ndl.gov.in

Sl.	Authority	Responsibilities	Communication Details
1	Ministry of Education (GoI), Department of Higher Education	Sanctioning Authority	https://www.education.gov.in/ict-initiatives
2	Indian Institute of Technology Kharagpur	Host Institute of the Project: The host institute of the project is responsible for providing infrastructure support and hosting the project	https://www.iitkgp.ac.in
3	National Digital Library of India Office, Indian Institute of Technology Kharagpur	The administrative and infrastructural headquarters of the project	Dr. B. Sutradhar bsutra@ndl.gov.in
4	Project PI / Joint PI	Principal Investigator and Joint Principal Investigators of the project	Dr. B. Sutradhar bsutra@ndl.gov.in Prof. Saswat Chakrabarti will be added soon
5	Website/Portal (Helpdesk)	Queries regarding NDLI and its services	support@ndl.gov.in
6	Contents and Copyright Issues	Queries related to content curation and copyright issues	content@ndl.gov.in
7	National Digital Library of India Club (NDLI Club)	Queries related to NDLI Club formation, support, user awareness program, seminar/symposium, collaboration, social media, promotion, and outreach	clubsupport@ndl.gov.in
8	Digital Preservation Centre (DPC)	Assistance with digitizing and archiving copyright-free printed books	dpc@ndl.gov.in
9	IDR Setup or Support	Queries related to establishment and support of Institutional Digital Repository (IDR) and IDR workshops	idr@ndl.gov.in