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1
Targeting of Swi/Snf to the yeast GAL1 UAS G requires the Mediator, TAF IIs, and RNA polymerase II.
EMBO J. 2004 Oct 13;23(20):4040-50. doi: 10.1038/sj.emboj.7600416. Epub 2004 Sep 23.
2
Variant histone H2A.Z, but not the HMG proteins Nhp6a/b, is essential for the recruitment of Swi/Snf, Mediator, and SAGA to the yeast GAL1 UAS(G).
Biochem Biophys Res Commun. 2008 May 16;369(4):1103-7. doi: 10.1016/j.bbrc.2008.02.144. Epub 2008 Mar 10.
3
Simultaneous recruitment of coactivators by Gcn4p stimulates multiple steps of transcription in vivo.
Mol Cell Biol. 2005 Jul;25(13):5626-38. doi: 10.1128/MCB.25.13.5626-5638.2005.
4
Interdependent recruitment of SAGA and Srb mediator by transcriptional activator Gcn4p.
Mol Cell Biol. 2005 May;25(9):3461-74. doi: 10.1128/MCB.25.9.3461-3474.2005.
6
SAGA is an essential in vivo target of the yeast acidic activator Gal4p.
Genes Dev. 2001 Aug 1;15(15):1935-45. doi: 10.1101/gad.911401.
7
Independent recruitment of mediator and SAGA by the activator Met4.
Mol Cell Biol. 2006 Apr;26(8):3149-63. doi: 10.1128/MCB.26.8.3149-3163.2006.
8
The Swi5 activator recruits the Mediator complex to the HO promoter without RNA polymerase II.
Genes Dev. 2001 Sep 15;15(18):2457-69. doi: 10.1101/gad.921601.
9
Recruitment of the Swi/Snf complex by Ste12-Tec1 promotes Flo8-Mss11-mediated activation of STA1 expression.
Mol Cell Biol. 2004 Nov;24(21):9542-56. doi: 10.1128/MCB.24.21.9542-9556.2004.
10
Mediator, TATA-binding protein, and RNA polymerase II contribute to low histone occupancy at active gene promoters in yeast.
J Biol Chem. 2014 May 23;289(21):14981-95. doi: 10.1074/jbc.M113.529354. Epub 2014 Apr 11.

引用本文的文献

2
Mediator recruits the cohesin loader Scc2 to RNA Pol II-transcribed genes and promotes sister chromatid cohesion.
Curr Biol. 2022 Jul 11;32(13):2884-2896.e6. doi: 10.1016/j.cub.2022.05.019. Epub 2022 Jun 1.
3
Capturing and Understanding the Dynamics and Heterogeneity of Gene Expression in the Living Cell.
Int J Mol Sci. 2020 Nov 5;21(21):8278. doi: 10.3390/ijms21218278.
4
Chromatin regulatory genes differentially interact in networks to facilitate distinct GAL1 activity and noise profiles.
Curr Genet. 2021 Apr;67(2):267-281. doi: 10.1007/s00294-020-01124-5. Epub 2020 Nov 7.
5
A functional genetic screen identifies the Mediator complex as essential for SSX2-induced senescence.
Cell Death Dis. 2019 Nov 6;10(11):841. doi: 10.1038/s41419-019-2068-1.
6
Quantitative imaging of chromatin decompaction in living cells.
Mol Biol Cell. 2018 Jul 15;29(13):1763-1777. doi: 10.1091/mbc.E17-11-0648. Epub 2018 May 17.
7
On the way of revealing coactivator complexes cross-talk during transcriptional activation.
Cell Biosci. 2016 Feb 24;6:15. doi: 10.1186/s13578-016-0081-y. eCollection 2016.
8
Histone Chaperone Nap1 Is a Major Regulator of Histone H2A-H2B Dynamics at the Inducible GAL Locus.
Mol Cell Biol. 2016 Mar 31;36(8):1287-96. doi: 10.1128/MCB.00835-15. Print 2016 Apr.
9
Med14 cooperates with brg1 in the differentiation of skeletogenic neural crest.
BMC Dev Biol. 2015 Nov 9;15:41. doi: 10.1186/s12861-015-0090-9.
10
Different Mechanisms Confer Gradual Control and Memory at Nutrient- and Stress-Regulated Genes in Yeast.
Mol Cell Biol. 2015 Nov;35(21):3669-83. doi: 10.1128/MCB.00729-15. Epub 2015 Aug 17.

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5
Independent recruitment in vivo by Gal4 of two complexes required for transcription.
Mol Cell. 2003 May;11(5):1301-9. doi: 10.1016/s1097-2765(03)00144-8.
8
The histone variant H3.3 marks active chromatin by replication-independent nucleosome assembly.
Mol Cell. 2002 Jun;9(6):1191-200. doi: 10.1016/s1097-2765(02)00542-7.
9
ATP-dependent nucleosome remodeling.
Annu Rev Biochem. 2002;71:247-73. doi: 10.1146/annurev.biochem.71.110601.135400. Epub 2001 Nov 9.
10
Transcription activator interactions with multiple SWI/SNF subunits.
Mol Cell Biol. 2002 Mar;22(6):1615-25. doi: 10.1128/MCB.22.6.1615-1625.2002.

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