Academic literature on the topic 'Yeast one-hybrid assay'

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Journal articles on the topic "Yeast one-hybrid assay"

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Okoye, Mercy E., Gerry L. Sexton, Eugene Huang, J. Michael McCaffery, and Prashant Desai. "Functional Analysis of the Triplex Proteins (VP19C and VP23) of Herpes Simplex Virus Type 1." Journal of Virology 80, no. 2 (2006): 929–40. http://dx.doi.org/10.1128/jvi.80.2.929-940.2006.

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ABSTRACT The triplex of herpesvirus capsids is a unique structural element. In herpes simplex virus type 1 (HSV-1), one molecule of VP19C and two of VP23 form a three-pronged structure that acts to stabilize the capsid shell through interactions with adjacent VP5 molecules. The interaction between VP19C and VP23 was inferred by yeast cryoelectron microscopy studies and subsequently confirmed by the two-hybrid assay. In order to define the functional domains of VP19C and VP23, a Tn7-based transposon was used to randomly insert 15 bp into the coding regions of these two proteins. The mutants wer
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Schulten, Hans-Jürgen, Wolfgang Engel, Karim Nayernia, and Peter Burfeind. "Yeast One-Hybrid Assay Identifies YY1 as a Binding Factor for a Proacrosin Promoter Element." Biochemical and Biophysical Research Communications 257, no. 3 (1999): 871–73. http://dx.doi.org/10.1006/bbrc.1999.0556.

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Chen, Gang, and Jumi A. Shin. "AhR/Arnt:XRE interaction: Turning false negatives into true positives in the modified yeast one-hybrid assay." Analytical Biochemistry 382, no. 2 (2008): 101–6. http://dx.doi.org/10.1016/j.ab.2008.07.026.

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Evans, David R. H., Kendra A. Swirsding, Bruce E. Taillon, and Jan F. Simons. "“One plate/three-reporter” assay format for the detection and validation of yeast two-hybrid interactions." BioTechniques 37, no. 5 (2004): 840–43. http://dx.doi.org/10.2144/04375pt02.

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Zhou, Zhong-xun, Bin He, Susan H. Hall, Elizabeth M. Wilson, and Frank S. French. "Domain Interactions between Coregulator ARA70 and the Androgen Receptor (AR)." Molecular Endocrinology 16, no. 2 (2002): 287–300. http://dx.doi.org/10.1210/mend.16.2.0765.

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Abstract The coregulator function of AR-associated protein 70 (ARA70) was investigated to further characterize its interaction with the AR. Using a yeast two-hybrid assay, androgen-dependent binding of ARA70 deletion mutants to the AR ligand-binding domain (LBD) was strongest with ARA70 amino acids 321–441 of the 614 amino acid ARA70 protein. Mutations adjacent to or within an FxxLF motif in this 120-amino acid region abolished androgen-dependent binding to the AR-LBD both in yeast and in glutathione-S-transferase affinity matrix assays. Yeast one-hybrid assays revealed an intrinsic ARA70 tran
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Wang, Dan, Changyue Jiang, Wandi Liu, and Yuejin Wang. "The WRKY53 transcription factor enhances stilbene synthesis and disease resistance by interacting with MYB14 and MYB15 in Chinese wild grape." Journal of Experimental Botany 71, no. 10 (2020): 3211–26. http://dx.doi.org/10.1093/jxb/eraa097.

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Abstract Resveratrol is notable not only for its functions in disease resistance in plants but also for its health benefits when it forms part of the human diet. Identification of new transcription factors helps to reveal the regulatory mechanisms of stilbene synthesis. Here, the WRKY53 transcription factor was isolated from the Chinese wild grape, Vitis quinquangularis. Vqwrky53 was expressed in a variety of tissues and responded to powdery mildew infection and to exogenous hormone application. VqWRKY53 was located in the nucleus and had transcriptional activation activity in yeast. A yeast t
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Saglam, Nihal Goren. "Identification of promoter DNA/protein interactions for MYB transcription factor in senescence using Yeast-One-Hybrid assay." Journal of Biotechnology 231 (August 2016): S20—S21. http://dx.doi.org/10.1016/j.jbiotec.2016.05.095.

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Huang, Kai, Tao Wu, Ziming Ma, et al. "Rice Transcription Factor OsWRKY55 Is Involved in the Drought Response and Regulation of Plant Growth." International Journal of Molecular Sciences 22, no. 9 (2021): 4337. http://dx.doi.org/10.3390/ijms22094337.

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WRKY transcription factors (TFs) have been reported to respond to biotic and abiotic stresses and regulate plant growth and development. However, the molecular mechanisms of WRKY TFs involved in drought stress and regulating plant height in rice remain largely unknown. In this study, we found that transgenic rice lines overexpressing OsWRKY55 (OsWRKY55-OE) exhibited reduced drought resistance. The OsWRKY55-OE lines showed faster water loss and greater accumulation of hydrogen peroxide (H2O2) and superoxide radical (O2−·) compared to wild-type (WT) plants under drought conditions. OsWRKY55 was
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Tang, Xuan, Junwei Shi, and Wubei Dong. "A yeast library-hybrid assay to screen maize- Rhizoctonia transcription factors and protein-protein interactions in one experimental pipeline." Agri Gene 1 (August 2016): 15–22. http://dx.doi.org/10.1016/j.aggene.2016.05.002.

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Schwartz, Katja, Kristy Richards, and David Botstein. "BIM1Encodes a Microtubule-binding Protein in Yeast." Molecular Biology of the Cell 8, no. 12 (1997): 2677–91. http://dx.doi.org/10.1091/mbc.8.12.2677.

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A previously uncharacterized yeast gene (YER016w) that we have named BIM1 (binding to microtubules) was obtained from a two-hybrid screen of a yeast cDNA library using as bait the entire coding sequence of TUB1 (encoding α-tubulin). Deletion of BIM1 results in a strong bilateral karyogamy defect, hypersensitivity to benomyl, and aberrant spindle behavior, all phenotypes associated with mutations affecting microtubules in yeast, and inviability at extreme temperatures (i.e., ≥37°C or ≤14°C). Overexpression of BIM1 in wild-type cells is lethal. A fusion of Bim1p with green fluorescent protein th
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Dissertations / Theses on the topic "Yeast one-hybrid assay"

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Rutter, Brian Douglas. "Catch of the Day: A yeast One-Hybrid Assay Identifies a Novel DNA-Binding Domain in Phytophthora Sojae." Bowling Green State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1339861904.

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Keymanesh, Keykhosrow. "The yeast-one-hybrid assay identifies LHCA2 and HSPRO2 as double-SORLIP1 element binding proteins in Arabidopsis thaliana." Thesis, California State University, Long Beach, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=1522636.

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<p> Early light induced proteins (ELIPs) are widely distributed in the plant kingdom. Members of the extended light harvesting complex (LHC) superfamily, <i> ELIP</i>s are expressed in the nucleus and the ELIP protein is transiently localized to the thylakoid membranes. Significant increase in expression of <i> ELIP</i>s has been reported in response to stresses such as high light, high and low temperature, exposure to UV and salinity. ELIP expression also increases at transitional stages of chloroplast development such as deetiolation, conversion to chromoplast, and senescence.</p><p> In se
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Chen, Gang. "A Modified Yeast One-hybrid Sytem to Investigate Protein-protein and Protein: DNA Interactions." Thesis, 2008. http://hdl.handle.net/1807/19337.

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A modified yeast one-hybrid (MY1H) system has been developed for in vivo investigation of simultaneous protein-protein and protein:DNA interactions. The traditional yeast one-hybrid assay (Y1H) permits examination of one expressed protein targeting one DNA site, whereas our MY1H allows coexpression of two different proteins and examination of their activity at the DNA target. This single-plasmid based MY1H was validated by use of the DNA-binding protein p53 and its inhibitory partners, large T antigen (LTAg) and 53BP2. The MY1H system could be used to examine proteins that contribute inhibitor
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Hurný, Andrej. "Transkripční regulace proteinu PIN4, membránového přenašeče rostlinného hormonu auxinu." Master's thesis, 2012. http://www.nusl.cz/ntk/nusl-310511.

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PIN-FORMED (PIN) proteins are plant-specific secondary transporters acting in the efflux of plant signaling molecule auxin from cells. Their asymmetrical localization within cells determines the directionality of auxin flow and thereby influences plant development. The activity of PIN proteins is regulated at multiple levels; however the primary step in the regulation of PIN proteins takes place at the level of gene transcription. Therefore the main focus of this diploma thesis is the characterization of the transcriptional regulation of PIN proteins, namely PIN4 protein. The observation of pl
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Book chapters on the topic "Yeast one-hybrid assay"

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Ji, Xiaoyu, Liuqiang Wang, Dandan Zang, and Yucheng Wang. "Transcription Factor-Centered Yeast One-Hybrid Assay." In Methods in Molecular Biology. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7871-7_11.

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Wanke, Dierk, and Klaus Harter. "Analysis of Plant Regulatory DNA sequences by the Yeast-One-Hybrid Assay." In Plant Signal Transduction. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-289-2_19.

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Reece-Hoyes, John S., and Albertha J. M. Walhout. "Gene-Centered Yeast One-Hybrid Assays." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-455-1_11.

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Gaudinier, Allison, Michelle Tang, Anne-Maarit Bågman, and Siobhan M. Brady. "Identification of Protein–DNA Interactions Using Enhanced Yeast One-Hybrid Assays and a Semiautomated Approach." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7003-2_13.

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Raychaudhuri, Soumya. "Protein Interaction Networks." In Computational Text Analysis. Oxford University Press, 2006. http://dx.doi.org/10.1093/oso/9780198567400.003.0017.

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Genes and proteins interact with each other in many complicated ways. For example, proteins can interact directly with each other to form complexes or to modify each other so that their function is altered. Gene expression can be repressed or induced by transcription factor proteins. In addition there are countless other types of interactions. They constitute the key physiological steps in regulating or initiating biological responses. For example the binding of transcription factors to DNA triggers the assembly of the RNA assembly machinery that transcribes the mRNA that then is used as the template for protein production. Interactions such as these have been carefully elucidated and have been described in great detail in the scientific literature. Modern assays such as yeast-2-hybrid screens offer rapid means to ascertain many of the potential protein–protein interactions in an organism in a large-scale approach. In addition, other experimental modalities such as gene-expression array assays offer indirect clues about possible genetic interactions. One area that has been greatly explored in the bioinformatics literature is the possibility of learning genetic or protein networks, both from the scientific literature and from large-scale experimental data. Indeed, as we get to know more and more genes, it will become increasingly important to appreciate their interactions with each other. An understanding of the interactions between genes and proteins in a network allows for a meaningful global view of the organism and its physiology and is necessary to better understand biology. In this chapter we will explore methods to either (1) mine the scientific literature to identify documented genetic interactions and build networks of genes or (2) to confirm protein interactions that have been proposed experimentally. Our focus here is on direct physical protein–protein interactions, though the techniques described could be extended to any type of biological interaction between genes or proteins. There are multiple steps that must be addressed in identifying genetic interaction information contained within the text. After compiling the necessary documents and text, the first step is to identify gene and protein names in the text.
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