Chromosomal location and tissue expression of the gene encoding the adenovirus E1A-regulated transcription factor E4F in humans and mice

1998 ◽  
Vol 9 (4) ◽  
pp. 320-323 ◽  
Author(s):  
Robert J. Rooney ◽  
Rachael R. Daniels ◽  
Nancy A. Jenkins ◽  
Debra J. Gilbert ◽  
Kristen Rothammer ◽  
...  
Genomics ◽  
1994 ◽  
Vol 20 (2) ◽  
pp. 203-209 ◽  
Author(s):  
Ralph Witzgall ◽  
Rüdiger Volk ◽  
Raymond S. Yeung ◽  
Joseph V. Bonventre

Genetics ◽  
1993 ◽  
Vol 133 (4) ◽  
pp. 999-1007
Author(s):  
R G Gregerson ◽  
L Cameron ◽  
M McLean ◽  
P Dennis ◽  
J Strommer

Abstract In most higher plants the genes encoding alcohol dehydrogenase comprise a small gene family, usually with two members. The Adh1 gene of Petunia has been cloned and analyzed, but a second identifiable gene was not recovered from any of three genomic libraries. We have therefore employed the polymerase chain reaction to obtain the major portion of a second Adh gene. From sequence, mapping and northern data we conclude this gene encodes ADH2, the major anaerobically inducible Adh gene of Petunia. The availability of both Adh1 and Adh2 from Petunia has permitted us to compare their structures and patterns of expression to those of the well-studied Adh genes of maize, of which one is highly expressed developmentally, while both are induced in response to hypoxia. Despite their evolutionary distance, evidenced by deduced amino acid sequence as well as taxonomic classification, the pairs of genes are regulated in strikingly similar ways in maize and Petunia. Our findings suggest a significant biological basis for the regulatory strategy employed by these distant species for differential expression of multiple Adh genes.


1994 ◽  
Vol 269 (15) ◽  
pp. 11663-11671
Author(s):  
S.L. Swendeman ◽  
C. Spielholz ◽  
N.A. Jenkins ◽  
D.J. Gilbert ◽  
N.G. Copeland ◽  
...  

2020 ◽  
Author(s):  
Seungwoo Cha ◽  
Chang Pyo Hong ◽  
Hyun Ah Kang ◽  
Ji-Sook Hahn

Abstract Gcr1, an important transcription factor for glycolytic genes in Saccharomyces cerevisiae, was recently revealed to have two isoforms, Gcr1U and Gcr1S, produced from un-spliced and spliced transcripts, respectively. In this study, by generating strains expressing only Gcr1U or Gcr1S using the CRISPR/Cas9 system, we elucidate differential activation mechanisms of these two isoforms. The Gcr1U monomer forms an active complex with its coactivator Gcr2 homodimer, whereas Gcr1S acts as a homodimer without Gcr2. The USS domain, 55 residues at the N-terminus existing only in Gcr1U, inhibits dimerization of Gcr1U and even acts in trans to inhibit Gcr1S dimerization. The Gcr1S monomer inhibits the metabolic switch from fermentation to respiration by directly binding to the ALD4 promoter, which can be restored by overexpression of the ALD4 gene, encoding a mitochondrial aldehyde dehydrogenase required for ethanol utilization. Gcr1U and Gcr1S regulate almost the same target genes, but show unique activities depending on growth phase, suggesting that these isoforms play differential roles through separate activation mechanisms depending on environmental conditions.


1989 ◽  
Vol 3 (12a) ◽  
pp. 1991-2002 ◽  
Author(s):  
U Muller ◽  
M P Roberts ◽  
D A Engel ◽  
W Doerfler ◽  
T Shenk

Endocrinology ◽  
1999 ◽  
Vol 140 (3) ◽  
pp. 1329-1337 ◽  
Author(s):  
Valeria R. Fantin ◽  
Brian E. Lavan ◽  
Qing Wang ◽  
Nancy A. Jenkins ◽  
Debra J. Gilbert ◽  
...  

2000 ◽  
Vol 11 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Irma S. Lantinga-van Leeuwen ◽  
Jan A. Mol ◽  
Hans S. Kooistra ◽  
Ad Rijnberk ◽  
Matthew Breen ◽  
...  

2009 ◽  
Vol 152 (1) ◽  
pp. 71-84 ◽  
Author(s):  
Ana-Rosa Ballester ◽  
Jos Molthoff ◽  
Ric de Vos ◽  
Bas te Lintel Hekkert ◽  
Diego Orzaez ◽  
...  

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