2007
DOI: 10.1016/j.jmb.2007.09.013
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Gal11p Dosage-compensates Transcriptional Activator Deletions via Taf14p

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Cited by 21 publications
(21 citation statements)
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“…We utilized the Split Ubiquitin assay to detect interactions between Gal11 and ScMSN2, ScMsn2-3DA, CgMSN2 or CgMsn2-3DA. In this assay, the interaction between Gal11 and Msn2 leads to the assembly of two halves of ubiquitin, each fused to the interacting proteins, that in turn leads to the degradation of the fused Ura3 protein (Lim et al, 2007). We found that both ScMsn2 and CgMsn2 can bind to Gal11, leading to a lower growth level of the respective strains, relative to the control strains on uracil-lacking plates (Fig.…”
Section: Msn2 Motif a And Motif B Are Essential For Msn2 And Gal11 Inmentioning
confidence: 74%
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“…We utilized the Split Ubiquitin assay to detect interactions between Gal11 and ScMSN2, ScMsn2-3DA, CgMSN2 or CgMsn2-3DA. In this assay, the interaction between Gal11 and Msn2 leads to the assembly of two halves of ubiquitin, each fused to the interacting proteins, that in turn leads to the degradation of the fused Ura3 protein (Lim et al, 2007). We found that both ScMsn2 and CgMsn2 can bind to Gal11, leading to a lower growth level of the respective strains, relative to the control strains on uracil-lacking plates (Fig.…”
Section: Msn2 Motif a And Motif B Are Essential For Msn2 And Gal11 Inmentioning
confidence: 74%
“…The split ubiquitin is a Y2H assay that is based on conditional proteolysis of ubiquitinated Ura3-conjugated proteins (Snider et al, 2010). This assay was extensively used to monitor interactions between membrane proteins and between transcriptional-activating domains, such as Gal4 and Gcn4, with other cellular proteins (Lim et al, 2007;Snider et al, 2010). We utilized the Split Ubiquitin assay to detect interactions between Gal11 and ScMSN2, ScMsn2-3DA, CgMSN2 or CgMsn2-3DA.…”
Section: Msn2 Motif a And Motif B Are Essential For Msn2 And Gal11 Inmentioning
confidence: 99%
“…TFIID induces DNA bending that may facilitate interactions between regulatory factors and promoters of their targets (52). Considering that Taf13p and Gcn4p physically interact (40), polymorphism within TAF13 plausibly affects the efficiency of transcription of Gcn4p target genes. Mbf1p is a coactivator of Gcn4p-dependent transcription (24).…”
Section: Discussionmentioning
confidence: 99%
“…6). Taf13p, a TATA binding protein-associated factor, is a subunit of TFIID that interacts with Gcn4p in vivo (40). We identified three nonsynonymous SNPs within the coding region of TAF13 between RM and S288c, a strain similar to BY: A137G, A138V, and G158A.…”
Section: Searching For Genetic Modulators Of Gcn4p-mediated Amino Acidmentioning
confidence: 98%
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