Journals / Turkish Journal of Biology / 2006 / Cilt: 30 - Sayı: 3

Non-Histone Proteins and the Mediator Complex are Essential for the Transcription of HXT2 and HXT4 Genes in Saccharomyces cerevisiae

Pages
163–169
Publication Date
2006-03-01
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this study, it was found that the transcription of HXT2 and HXT4 genes decreased 4- to 7-fold in the yeast strain that does not contain the non-histone proteins 6A and 6B (Nhp6A/B).

📌 3 Key Takeaways

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Objective & Hypothesis:Transcriptional activation of HXT2 and HXT4 genes require rapid reorganization of the chromatin structure on the promoter regions of these genes.
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Key Findings & Data:In this study, it was found that the transcription of HXT2 and HXT4 genes decreased 4- to 7-fold in the yeast strain that does not contain the non-histone proteins 6A and 6B (Nhp6A/B).
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Conclusion & Impact:These results indicated that Nhp6A/B and the mediator complex are essential for the regulation of HXT2 and HXT4 gene transcription in S. cerevisiae.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Saccharomyces cerevisiae · glucose repression · hexose transporters

Abstract

Transcriptional activation of HXT2 and HXT4 genes require rapid reorganization of the chromatin structure on the promoter regions of these genes. In this study, it was found that the transcription of HXT2 and HXT4 genes decreased 4- to 7-fold in the yeast strain that does not contain the non-histone proteins 6A and 6B (Nhp6A/B). In addition, results of this research indicated that Nhp6A/B are required for the rapid derepression and activation of HXT2 and HXT4 transcription upon glucose signaling. Furthermore, it was found that Med2p, which provides the connection between the transcriptional activators and the basal transcription factors, is also required for the activation of HXT2 and HXT4 transcription. Transcription of HXT2 and HXT4 decreased 2- to 13-fold in Med2 mutant S. cerevisiae cells. These results indicated that Nhp6A/B and the mediator complex are essential for the regulation of HXT2 and HXT4 gene transcription in S. cerevisiae.

Özet

Transcriptional activation of HXT2 and HXT4 genes require rapid reorganization of the chromatin structure on the promoter regions of these genes. In this study, it was found that the transcription of HXT2 and HXT4 genes decreased 4- to 7-fold in the yeast strain that does not contain the non-histone proteins 6A and 6B (Nhp6A/B). In addition, results of this research indicated that Nhp6A/B are required for the rapid derepression and activation of HXT2 and HXT4 transcription upon glucose signaling. Furthermore, it was found that Med2p, which provides the connection between the transcriptional activators and the basal transcription factors, is also required for the activation of HXT2 and HXT4 transcription. Transcription of HXT2 and HXT4 decreased 2- to 13-fold in Med2 mutant S. cerevisiae cells. These results indicated that Nhp6A/B and the mediator complex are essential for the regulation of HXT2 and HXT4 gene transcription in S. cerevisiae.

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Cite This Article

GÜZELVARDAR, S., TÜRKEL, S. (2006). Non-Histone Proteins and the Mediator Complex are Essential for the Transcription of HXT2 and HXT4 Genes in Saccharomyces cerevisiae. Turkish Journal of Biology, Cilt: 30 - Sayı: 3, 163–169. https://ajindex.com/articles/182249

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References (13)

  1. Boles E, Hollenberg CP. The molecular genetics of hexose transport in yeasts. FEMS Microbiol. Rev. 21: 85-111, 1997.
  2. Özcan S, Johnston M. Three different regulatory mechanisms enable yeast hexose transporter (HXT) genes to be induced by different levels of glucose. Mol. Cell. Biol. 15: 1564-1572, 1995.
  3. Kolodrubetz D, Burgum A. Duplicated NHP6 genes of Saccharomyces cerevisiae encode proteins homologous to bovine high mobility group protein 1. J. Biol. Chem. 265: 3234-3239, 1990. 8. Paull TT, Johnson RC. DNA looping by Saccharomyces cerevisiae high mobility group proteins Nhp6A/B. J. Biol. Chem. 270: 8744- 8754, 1995.
  4. Moreira JMA, Holmberg S. Chromatin-mediated transcriptional regulation by the yeast architectural factors Nhp6A and Nhp6B. EMBO J. 19: 6804-6813, 2000.
  5. Wu JPY, Ruhlmann C, Winston F et al. Molecular architecture of the S. cerevisiae SAGA complex. Molecular Cell 15: 199-208, 2004.
  6. Sterner DE, Grant PA, Roberts SM et al. Functional organization of the yeast SAGA complex: Distinct components involved in structural integrity, nucleosome acetylation, and TATA-binding protein interaction. Mol. Cell. Biol. 19: 86-98, 1999.
  7. Yu Y, Eriksson P, Stillman DJ. Architectural transcription factors and the SAGA complex function in parallel pathways to activate transcription. Mol. Cell. Biol. 20: 2350-2357, 2000.
  8. Malik S, Roeder RG. Transcriptional regulation through mediator- like coactivators in yeast and metazoan cells. Trends Biochem. Sci. 25: 277-283, 2000. Guglielmi B, van Berkum NL, Klapholz B et al. A high resolution protein interaction map of the yeast mediator complex. Nucleic Acids Res. 32: 5379-5391, 2004.
  9. Brachmann CB, Davies A, Cost G Jet al. Designer deletion strains derived from Saccharomyces cerevisiae S288C: A useful set of strains and plasmids for PCR-mediated gene disruption and other applications. Yeast 14: 115-132, 1998.
  10. Kruckeberg AL, Bisson LF. The HXT2 gene of Saccharomyces cerevisiae is required for high-affinity glucose transport. Mol. Cell. Biol. 10: 5903-5913, 1990.
  11. Theodoris G, Fong NM, Coons DM et al. High-copy suppression of glucose transport defect by HXT4 and regulatory elements in the promoters of the HXT genes in Saccharomyces cerevisiae. Genetics 137: 957-966, 1994.
  12. Türkel S, Turgut T, Lopez MC et al. Mutations in GCR1 affect SUC2 gene expression in Saccharomyces cerevisiae. Mol. Gen. Genomics 268: 825-831, 2003.
  13. Sarokin L, Carlson M. Upstream region of the SUC2 gene confers regulated expression to a heterologous gene in Sac