FBP1/YLR377C Literature Guide Help

Other names published for FBP1: ACN8, fructose 1,6-bisphosphate 1-phosphatase, YLR377C

FBP1 - RNA Levels and Processing (23)

ReferenceOther Genes Addressed
Duenas-Sanchez R, et al.  (2012) Transcriptional regulation of fermentative and respiratory metabolism in Saccharomyces cerevisiae industrial bakers' strains. FEMS Yeast Res 12(6):625-36
Soontorngun N, et al.  (2012) Genome-wide location analysis reveals an important overlap between the targets of the yeast transcriptional regulators Rds2 and Adr1. Biochem Biophys Res Commun 423(4):632-7
Young ET, et al.  (2012) The AMP-activated protein kinase Snf1 regulates transcription factor binding, RNA polymerase II activity, and mRNA stability of glucose-repressed genes in Saccharomyces cerevisiae. J Biol Chem 287(34):29021-34
Raab AM, et al.  (2011) Shifting the Fermentative/Oxidative Balance in Saccharomyces cerevisiae by Transcriptional Deregulation of Snf1 via Overexpression of the Upstream Activating Kinase Sak1p. Appl Environ Microbiol 77(6):1981-9
Wang J, et al.  (2010) Gene regulatory changes in yeast during life extension by nutrient limitation. Exp Gerontol 45(7-8):621-31
Lorenz DR, et al.  (2009) A network biology approach to aging in yeast. Proc Natl Acad Sci U S A 106(4):1145-50
Roberts GG 3rd and Hudson AP  (2009) Rsf1p is required for an efficient metabolic shift from fermentative to glycerol-based respiratory growth in S. cerevisiae. Yeast 26(2):95-110
Biddick RK, et al.  (2008) Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes. PLoS One 3(1):e1436
Bonander N, et al.  (2008) Transcriptome analysis of a respiratory Saccharomycescerevisiae strain suggests the expression of its phenotype is glucose insensitive and predominantly controlled by Hap4, Cat8 and Mig1. BMC Genomics 9:365
Jin C, et al.  (2007) SIT4 regulation of Mig1p-mediated catabolite repression in Saccharomyces cerevisiae. FEBS Lett 581(29):5658-63
Kitanovic A and Wolfl S  (2006) Fructose-1,6-bisphosphatase mediates cellular responses to DNA damage and aging in Saccharomyces cerevisiae. Mutat Res 594(1-2):135-47
Tanaka F, et al.  (2006) Functional genomic analysis of commercial baker's yeast during initial stages of model dough-fermentation. Food Microbiol 23(8):717-28
Panadero J, et al.  (2005) Validation of a flour-free model dough system for throughput studies of baker's yeast. Appl Environ Microbiol 71(3):1142-7
Andalis AA, et al.  (2004) Defects arising from whole-genome duplications in Saccharomyces cerevisiae. Genetics 167(3):1109-21
Banerjee D, et al.  (2004) Genome-wide expression profile of steroid response in Saccharomyces cerevisiae. Biochem Biophys Res Commun 317(2):406-13
Otterstedt K, et al.  (2004) Switching the mode of metabolism in the yeast Saccharomyces cerevisiae. EMBO Rep 5(5):532-7
Parveen M, et al.  (2004) Response of Saccharomyces cerevisiae to a monoterpene: evaluation of antifungal potential by DNA microarray analysis. J Antimicrob Chemother 54(1):46-55
Boer VM, et al.  (2003) The genome-wide transcriptional responses of Saccharomyces cerevisiae grown on glucose in aerobic chemostat cultures limited for carbon, nitrogen, phosphorus, or sulfur. J Biol Chem 278(5):3265-74
Bro C, et al.  (2003) Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells. J Biol Chem 278(34):32141-9
Kang JJ, et al.  (2000) Transcript quantitation in total yeast cellular RNA using kinetic PCR. Nucleic Acids Res 28(2):e2
Yin Z, et al.  (2000) Differential post-transcriptional regulation of yeast mRNAs in response to high and low glucose concentrations. Mol Microbiol 35(3):553-65
Aranda A, et al.  (1998) Transcription termination downstream of the Saccharomyces cerevisiae FBP1 [changed from FPB1] poly(A) site does not depend on efficient 3'end processing. RNA 4(3):303-18
Mercado JJ, et al.  (1994) The levels of yeast gluconeogenic mRNAs respond to environmental factors. Eur J Biochem 224(2):473-81