Literature DB >> 2944600

An adenovirus E1a protein region required for transformation and transcriptional repression.

J W Lillie, M Green, M R Green.   

Abstract

The adenovirus E1a region encodes two closely related gene products: 243 and 289 amino acid phosphoproteins. These proteins differ in their primary sequence only by 46 amino acids unique to the 289 amino acid protein. By constructing single-base substitution mutants we localized two functional regions of these E1a proteins: one required for efficient transcriptional activation, another required for efficient transcriptional repression. The 289 amino acid protein contains both regions and appears to function primarily as a transcriptional activator. The 243 amino acid protein lacks the transcriptional activation domain and appears to function primarily as a transcriptional repressor. Mutations within a highly conserved region define a novel class of transformation-defective mutants. These mutant E1a proteins can still efficiently activate transcription of early viral and cellular genes but cannot repress transcription of target genes. The fact that viral transformation may require a transcriptional repression function provides new insights into the mechanism by which adenovirus transforms cells.

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Year:  1986        PMID: 2944600     DOI: 10.1016/0092-8674(86)90704-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  153 in total

1.  The ORF RTL1 transcript of fowl adenovirus type-8 is spliced and truncated at late stages of the virus replication cycle.

Authors:  J X Cao; P J Krell; E Nagy
Journal:  Virus Genes       Date:  2000       Impact factor: 2.332

2.  Adenovirus infection of differentiated F9 cells results in a global shut-off of differentiation-induced gene expression.

Authors:  R J Weigel; J R Nevins
Journal:  Nucleic Acids Res       Date:  1990-10-25       Impact factor: 16.971

3.  Transcriptional regulation of the human glycoprotein hormone common alpha subunit gene by cAMP-response-element-binding protein (CREB)-binding protein (CBP)/p300 and p53.

Authors:  Xian Zhang; Roger J A Grand; Christopher J McCabe; Jayne A Franklyn; Phillip H Gallimore; Andrew S Turnell
Journal:  Biochem J       Date:  2002-11-15       Impact factor: 3.857

4.  Induction of AP-1 DNA-binding activity and c-fos mRNA by the adenovirus 243R E1A protein and cyclic AMP requires domains necessary for transformation.

Authors:  R W Gedrich; S T Bayley; D A Engel
Journal:  J Virol       Date:  1992-10       Impact factor: 5.103

5.  Promoter-specific trans-activation by the adenovirus E1A12S product involves separate E1A domains.

Authors:  V B Kraus; E Moran; J R Nevins
Journal:  Mol Cell Biol       Date:  1992-10       Impact factor: 4.272

6.  Structure-function analysis of the human papillomavirus type 16 E7 oncoprotein.

Authors:  W C Phelps; K Münger; C L Yee; J A Barnes; P M Howley
Journal:  J Virol       Date:  1992-04       Impact factor: 5.103

7.  Interaction of a common factor with ATF, Sp1, or TATAA promoter elements is required for these sequences to mediate transactivation by the adenoviral oncogene E1a.

Authors:  S J Weintraub; D C Dean
Journal:  Mol Cell Biol       Date:  1992-02       Impact factor: 4.272

8.  Distinguishable promoter elements are involved in transcriptional activation by E1a and cyclic AMP.

Authors:  K A Lee; J S Fink; R H Goodman; M R Green
Journal:  Mol Cell Biol       Date:  1989-10       Impact factor: 4.272

9.  Molecular characterization of the cysJIH promoters of Salmonella typhimurium and Escherichia coli: regulation by cysB protein and N-acetyl-L-serine.

Authors:  J Ostrowski; N M Kredich
Journal:  J Bacteriol       Date:  1989-01       Impact factor: 3.490

10.  Complementary functions of E1a conserved region 1 cooperate with conserved region 3 to activate adenovirus serotype 5 early promoters.

Authors:  H K Wong; E B Ziff
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

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