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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

AMN1 Amn1p

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Top mentioned proteins: CAN, ACID, CIs, HAD, V1a
Papers on AMN1
Integrated genomic and functional analyses of histone demethylases identify oncogenic KDM2A isoform in breast cancer.
Yang et al., Jilin, China. In Mol Carcinog, Aug 2015
KDM2A has two isoforms: the long isoform is comprised of a JmjC domain, CXXC-zinc finger, PHD zinc finger, F-box, and the AMN1 protein domain; whereas the short isoform of KDM2A lacks the N-terminal JmjC domain but contains all other motifs.
The role of the F-box gene TaFBA1 from wheat (Triticum aestivum L.) in drought tolerance.
Wang et al., Tai'an, China. In Plant Physiol Biochem, 2014
TaFBA1 encodes a putative 325-amino-acid F-box protein with a conserved N-terminal F-box domain and a C-terminal AMN1 domain.
Polygenic molecular architecture underlying non-sexual cell aggregation in budding yeast.
Luo et al., Shanghai, China. In Dna Res, 2013
High-resolution mapping following up with knockout and allele replacement experiments resolved the QTL into the underlying genes (AMN1, RGA1, FLO1, and FLO8) or even into the causative nucleotide.
Generation of stable, non-aggregating Saccharomyces cerevisiae wild isolates.
Majewska et al., Kraków, Poland. In Acta Biochim Pol, 2012
This is achieved by replacing the native allele of the AMN1 gene with an allele found in the W303 laboratory strain.
Lysine-specific demethylase 2A (KDM2A) normalizes human embryonic stem cell derived keratinocytes.
Green et al., Boston, United States. In Proc Natl Acad Sci U S A, 2012
This (KDM2A-N782) encodes the 782AA protein containing the JmjC, CXXC, and Ring domains, but not the F-box and AMN1 domains, unlike KDM2A, which has been studied by other groups.
Genetic analysis of variation in transcription factor binding in yeast.
Snyder et al., New Haven, United States. In Nature, 2010
We also identified two trans-factors, AMN1 and FLO8, that modulate Ste12 binding to promoters of more than ten genes under alpha-factor treatment.
A Bayesian partition method for detecting pleiotropic and epistatic eQTL modules.
Liu et al., Stamford, United States. In Plos Comput Biol, 2010
We demonstrated that one of the novel modules containing many daughter-cell expressed genes is regulated by AMN1 and BPH1.
Gene expression profiling in cells with enhanced gamma-secretase activity.
Fraering et al., Lausanne, Switzerland. In Plos One, 2008
Among the 21 validated genes, the strikingly decreased transcription of PTPRG and AMN1 and increased transcription of UPP1 potentially support data on cell cycle disturbances relevant to cancer, stem cell and neurodegenerative diseases' research.
Detection of eQTL modules mediated by activity levels of transcription factors.
Li et al., Los Angeles, United States. In Bioinformatics, 2007
They are organized into 4 eQTL modules: an amino acid synthesis module featuring a cis-linked gene LEU2 and the mediating TF Leu3; a pheromone response module featuring a cis-linked gene GPA1 and the mediating TF Ste12; an energy-source control module featuring two cis-linked genes, GSY2 and HAP1, and the mediating TF Hap1; a mitotic exit module featuring four cis-linked genes, AMN1, CSH1, DEM1 and TOS1, and the mediating TF complex Ace2/Swi5.
Direct in vivo access to potential gene targets of the RPD3 histone deactylase using fitness-based interferential genetics.
Daniel, Gif-sur-Yvette, France. In Yeast, 2007
Moreover, other selected genes are linked to cell-cycle control (CSE4, AMN1, VAC17 and GRR1).
Budding yeast DNA damage adaptation mutants exhibit defects in mitotic exit.
Wang et al., Tallahassee, United States. In Cell Cycle, 2006
cdc5-ad mutant cells are sensitive to high dosage of Amn1, a negative regulator of MEN.
Local regulatory variation in Saccharomyces cerevisiae.
Kruglyak et al., Seattle, United States. In Plos Genet, 2005
We also experimentally confirmed one example in which local regulatory variation in the gene AMN1 acts in trans through a feedback loop.
Trans-acting regulatory variation in Saccharomyces cerevisiae and the role of transcription factors.
Kruglyak et al., Seattle, United States. In Nat Genet, 2003
Positional cloning and functional assays showed that polymorphisms in GPA1 and AMN1 affect expression of genes involved in pheromone response and daughter cell separation, respectively.
Exit from exit: resetting the cell cycle through Amn1 inhibition of G protein signaling.
Elledge et al., Houston, United States. In Cell, 2003
We find that daughter cells activate an Antagonist of MEN pathway (AMEN) in part through induction of the Amn1 protein that binds directly to Tem1 and prevents its association with its target kinase Cdc15.
Sequencing and functional analysis of the Hansenula polymorpha genomic fragment containing the YPT1 and PMI40 genes.
Kang et al., Taejŏn, South Korea. In Yeast, 2002
The genomic fragment contains four open reading frames homologous to the Saccharomyces cerevisiae genes YPT1 (which codes for a GTP-binding protein; 75% amino acid identity), PMI40 (encoding phosphomannose isomerase; 61% identity), YLR065c (30% identity) and CST13 (28% identity).
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