scholarly journals ABSCISIC ACID INSENSITIVE3 regulates abscisic acid-responsive gene expression with the nuclear factor Y complex through the ACTT-core element inPhyscomitrella patens

2013 ◽  
Vol 199 (1) ◽  
pp. 101-109 ◽  
Author(s):  
Izumi Yotsui ◽  
Masashi Saruhashi ◽  
Takahiro Kawato ◽  
Teruaki Taji ◽  
Takahisa Hayashi ◽  
...  
Keyword(s):  
Gene Expression ◽  
Abscisic Acid ◽  
Nuclear Factor ◽  
Core Element ◽  
Nuclear Factor Y ◽  
Responsive Gene ◽  
Abscisic Acid Insensitive3

scholarly journals A Homeodomain Leucine Zipper Gene from Craterostigma plantagineum Regulates Abscisic Acid Responsive Gene Expression and Physiological Responses

2006 ◽  
Vol 61 (3) ◽  
pp. 469-489 ◽  
Author(s):  
Xin Deng ◽  
Jonathan Phillips ◽  
Anne Bräutigam ◽  
Peter Engström ◽  
Henrik Johannesson ◽  
...  
Keyword(s):  
Gene Expression ◽  
Abscisic Acid ◽  
Leucine Zipper ◽  
Physiological Responses ◽  
Craterostigma Plantagineum ◽  
Responsive Gene

scholarly journals CCAAT/Enhancer Binding Protein and Nuclear Factor-Y Regulate Adiponectin Gene Expression in Adipose Tissue

Diabetes ◽  
2004 ◽  
Vol 53 (11) ◽  
pp. 2757-2766 ◽  
Author(s):  
S.-k. Park ◽  
S.-Y. Oh ◽  
M.-Y. Lee ◽  
S. Yoon ◽  
K.-S. Kim ◽  
...  
Keyword(s):  
Gene Expression ◽  
Adipose Tissue ◽  
Binding Protein ◽  
Nuclear Factor ◽  
Adiponectin Gene ◽  
Nuclear Factor Y ◽  
Enhancer Binding Protein ◽  
Ccaat Enhancer Binding Protein

scholarly journals DREB2C Interacts with ABF2, a bZIP Protein Regulating Abscisic Acid-Responsive Gene Expression, and Its Overexpression Affects Abscisic Acid Sensitivity

2010 ◽  
Vol 153 (2) ◽  
pp. 716-727 ◽  
Author(s):  
Sun-ji Lee ◽  
Jung-youn Kang ◽  
Hee-Jin Park ◽  
Myoung Duck Kim ◽  
Min Seok Bae ◽  
...  
Keyword(s):  
Gene Expression ◽  
Abscisic Acid ◽  
Acid Sensitivity ◽  
Bzip Protein ◽  
Responsive Gene

scholarly journals Nuclear Factor-Y is an adipogenic factor that regulates leptin gene expression

2015 ◽  
Vol 4 (5) ◽  
pp. 392-405 ◽  
Author(s):  
Yi-Hsueh Lu ◽  
Olof Stefan Dallner ◽  
Kivanc Birsoy ◽  
Gulya Fayzikhodjaeva ◽  
Jeffrey M. Friedman
Keyword(s):  
Gene Expression ◽  
Nuclear Factor ◽  
Nuclear Factor Y

scholarly journals Identification, Structural Characterization and Gene Expression Analysis of Members of the Nuclear Factor-Y Family in Chickpea (Cicer arietinum L.) under Dehydration and Abscisic Acid Treatments

2018 ◽  
Vol 19 (11) ◽  
pp. 3290 ◽  
Author(s):  
Ha Chu ◽  
Kien Nguyen ◽  
Yasuko Watanabe ◽  
Dung Le ◽  
Thu Pham ◽  
...  
Keyword(s):  
Abscisic Acid ◽  
In Silico ◽  
Major Gene ◽  
Expression Patterns ◽  
Dependent Manner ◽  
Nuclear Factor ◽  
Nuclear Factor Y ◽  
Fundamental Information ◽  
Close Relationship ◽  
In Silico Analyses

In plants, the Nuclear Factor-Y (NF-Y) transcription factors (TFs), which include three distinct types of NF-YA, NF-YB, and NF-YC TFs, have been identified to play key roles in the regulation of various plant growth and developmental processes under both normal and environmental stress conditions. In this work, a total of 40 CaNF-Y-encoding genes, including eight CaNF-YAs, 21 CaNF-YBs, and 11 CaNF-YCs, were identified in chickpea, and their major gene and protein characteristics were subsequently obtained using various web-based tools. Of our interest, a phylogenetically-based analysis predicted 18 CaNF-Ys (eight CaNF-YAs, seven CaNF-YBs, and three CaNF-YCs) that potentially play roles in chickpea responses to dehydration according to their close relationship with the well-characterized GmNF-Ys in soybean. These results were in good agreement with the enrichment of drought-responsive cis-regulatory motifs and expression patterns obtained from in silico analyses using publically available transcriptome data. Most of the phylogenetically predicted drought-responsive CaNF-Y genes (15 of 18) were quantitatively validated to significantly respond to dehydration treatment in leaves and/or roots, further supporting the results of in silico analyses. Among these CaNF-Y genes, the transcript levels of CaNF-YA01 and CaNF-YC10 were the most highly accumulated in leaves (by approximately eight-fold) and roots (by approximately 18-fold), respectively, by dehydration. Furthermore, 12 of the 18 CaNF-Y genes were found to be responsive to the most well-known stress hormone, namely abscisic acid (ABA), in leaves and/or roots, suggesting that these genes may act in chickpea response to dehydration in ABA-dependent manner. Taken together, our study has provided a comprehensive and fundamental information for further functional analyses of selected CaNF-Y candidate genes, ultimately leading to the improvement of chickpea growth under water-limited conditions.

Abscisic Acid in Abiotic Stress‐responsive Gene Expression

2019 ◽  
pp. 145-184
Author(s):  
Liliane Souza Conceição Tavares ◽  
Sávio Pinho Reis ◽  
Deyvid Novaes Marques ◽  
Eraldo José Madureira Tavares ◽  
Solange Cunha Ferreira ◽  
...  
Keyword(s):  
Gene Expression ◽  
Abscisic Acid ◽  
Abiotic Stress ◽  
Responsive Gene

scholarly journals Expression of the rat liver carnitine palmitoyltransferase I (CPT-Iα) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization

1999 ◽  
Vol 340 (2) ◽  
pp. 425-432 ◽  
Author(s):  
Michelle L. STEFFEN ◽  
Wilbur R. HARRISON ◽  
Frederick F. B. ELDER ◽  
George A. COOK ◽  
Edwards A. PARK
Keyword(s):  
Gene Expression ◽  
Carnitine Palmitoyltransferase ◽  
Chromosome 1 ◽  
Proximal Promoter ◽  
Nuclear Factor ◽  
Membrane Expression ◽  
Base Pairs ◽  
Nuclear Factor Y ◽  
Specific Regulation ◽  
Cpt I

Carnitine palmitoyltransferase (CPT)-I catalyses the transfer of long-chain fatty acids from CoA to carnitine for translocation across the mitochondrial inner membrane. Expression of the ‘liver’ isoform of the CPT-I gene (CPT-Iα) is subject to developmental, hormonal and tissue-specific regulation. To understand the basis for control of CPT-Iα gene expression, we have characterized the proximal promoter of the CPT-Iα gene. Here, we report the sequence of 6839 base pairs of the promoter and the localization of the rat CPT-Iα gene to region q43 on chromosome 1. Our studies show that the first 200 base pairs of the promoter are sufficient to drive transcription of the CPT-Iα gene. Within this region are two sites that bind both Sp1 and Sp3 transcription factors. In addition, nuclear factor Y (NF-Y) binds the proximal promoter. Mutation at the Sp1 or NF-Y sites severely decreases transcription from the CPT-Iα promoter. Other protein binding sites were identified within the first 200 base pairs of the promoter by DNase I footprinting, and these elements contribute to CPT-Iα gene expression. Our studies demonstrate that CPT-Iα is a TATA-less gene which utilizes NF-Y and Sp proteins to drive basal expression.

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