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CDC36  -  CCR4-NOT core subunit CDC36

Saccharomyces cerevisiae S288c

Synonyms: DNA19, General negative regulator of transcription subunit 2, NOT2, YDL165W, cell division cycle protein 36
 
 
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High impact information on CDC36

  • However, estrogen had no effect on late G1 arrest induced by the alpha factor or ts mutation of cdc36 [1].
  • CDC4 and CDC36 are Saccharomyces cerevisiae cell division cycle genes, while ets is a transformation-specific sequence of avian erythroblastosis virus E26 [2].
  • We report here significant primary sequence homology among the predicted translational products of three genes: CDC4 , CDC36 and ets [2].
  • Allele-specific suppression, a two-hybrid interaction, and biochemical confractionation suggest that NOT1 and NOT2 are nuclear proteins associated in a discrete, 500-kD complex [3].
  • This suggests that association of Not2 with the Ada/Gcn5 histone acetyltransferase complex is involved in regulation of the HIS3 promoter [4].
 

Biological context of CDC36

 

Physical interactions of CDC36

  • The not2::R165G also abrogated NOT2 ability to interact with ADA2 but had little effect on the integrity of the CCR4-NOT complex [9].
 

Regulatory relationships of CDC36

  • Overexpression of MOT2 suppresses the growth defect of temperature-sensitive mutations in CDC36 and CDC39 [5].
 

Other interactions of CDC36

  • The coding regions corresponding to CDC36, CDC37, and CDC39 were then identified and localized by R-loop analysis [10].
  • The CDC9 gene of Saccharomyces cerevisiae encodes a DNA ligase, and we have determined the nucleotide sequence of a 3.85 kb fragment of DNA which encompasses the convergently transcribed CDC9 and CDC36 genes [11].
  • Alterations in NOT2 contacts to ADA2, therefore, do not necessarily result in effects on the CCR4-NOT complex nor result in severe growth defects [9].
  • In contrast, the not2-4 allele destabilized the CCR4-NOT complex to a lesser extent and had no effect on NOT5 association with NOT2 [9].
  • Alpha-factor-treated cells arrested in a thermosensitive state, as did the temperature-sensitive mutant cdc36 when grown at the restrictive temperature. cdc7, which arrested at the G1-S boundary, arrested in a thermosensitive state [12].

References

  1. Estrogen can regulate the cell cycle in the early G1 phase of yeast by increasing the amount of adenylate cyclase mRNA. Tanaka, S., Hasegawa, S., Hishinuma, F., Kurata, S. Cell (1989) [Pubmed]
  2. A relationship between the yeast cell cycle genes CDC4 and CDC36 and the ets sequence of oncogenic virus E26. Peterson, T.A., Yochem, J., Byers, B., Nunn, M.F., Duesberg, P.H., Doolittle, R.F., Reed, S.I. Nature (1984) [Pubmed]
  3. NOT1(CDC39), NOT2(CDC36), NOT3, and NOT4 encode a global-negative regulator of transcription that differentially affects TATA-element utilization. Collart, M.A., Struhl, K. Genes Dev. (1994) [Pubmed]
  4. Association of distinct yeast Not2 functional domains with components of Gcn5 histone acetylase and Ccr4 transcriptional regulatory complexes. Benson, J.D., Benson, M., Howley, P.M., Struhl, K. EMBO J. (1998) [Pubmed]
  5. The yeast MOT2 gene encodes a putative zinc finger protein that serves as a global negative regulator affecting expression of several categories of genes, including mating-pheromone-responsive genes. Irie, K., Yamaguchi, K., Kawase, K., Matsumoto, K. Mol. Cell. Biol. (1994) [Pubmed]
  6. CDC36 and CDC39 are negative elements in the signal transduction pathway of yeast. Neiman, A.M., Chang, F., Komachi, K., Herskowitz, I. Cell Regul. (1990) [Pubmed]
  7. Nucleotide sequence of the yeast cell division cycle start genes CDC28, CDC36, CDC37, and CDC39, and a structural analysis of the predicted products. Ferguson, J., Ho, J.Y., Peterson, T.A., Reed, S.I. Nucleic Acids Res. (1986) [Pubmed]
  8. Pachytene arrest and other meiotic effects of the start mutations in Saccharomyces cerevisiae. Shuster, E.O., Byers, B. Genetics (1989) [Pubmed]
  9. Characterization of mutations in NOT2 indicates that it plays an important role in maintaining the integrity of the CCR4-NOT complex. Russell, P., Benson, J.D., Denis, C.L. J. Mol. Biol. (2002) [Pubmed]
  10. Isolation and transcriptional characterization of three genes which function at start, the controlling event of the Saccharomyces cerevisiae cell division cycle: CDC36, CDC37, and CDC39. Breter, H.J., Ferguson, J., Peterson, T.A., Reed, S.I. Mol. Cell. Biol. (1983) [Pubmed]
  11. The nucleotide sequence of the DNA ligase gene (CDC9) from Saccharomyces cerevisiae: a gene which is cell-cycle regulated and induced in response to DNA damage. Barker, D.G., White, J.H., Johnston, L.H. Nucleic Acids Res. (1985) [Pubmed]
  12. Effect of cell cycle position on thermotolerance in Saccharomyces cerevisiae. Plesset, J., Ludwig, J.R., Cox, B.S., McLaughlin, C.S. J. Bacteriol. (1987) [Pubmed]
 
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