DNA damage response element gene transcriptions: Difference between revisions

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# inverse complement, positive strand, negative direction, looking for 5'-ATTGAAA-3', 0.
# inverse complement, positive strand, negative direction, looking for 5'-ATTGAAA-3', 0.
# inverse complement, positive strand, positive direction, looking for 5'-ATTGAAA-3', 0.
# inverse complement, positive strand, positive direction, looking for 5'-ATTGAAA-3', 0.
# inverse negative strand, negative direction, looking for 5'-AAAAAAAA-3', 0.
# inverse negative strand, negative direction, looking for 5'-TAACTTT-3', 0.
# inverse negative strand, positive direction, looking for 5'-AAAAAAAA-3', 0.
# inverse negative strand, positive direction, looking for 5'-TAACTTT-3', 0.
# inverse positive strand, negative direction, looking for 5'-AAAAAAAA-3', 0.
# inverse positive strand, negative direction, looking for 5'-TAACTTT-3', 0.
# inverse positive strand, positive direction, looking for 5'-AAAAAAAA-3', 0.
# inverse positive strand, positive direction, looking for 5'-TAACTTT-3', 0.
 
=== DDRE core promoters===
{{main|Core promoter gene transcriptions}}
 
=== DDRE proximal promoters===
{{main|Proximal promoter gene transcriptions}}
 
=== DDRE distal promoters===
{{main|Distal promoter gene transcriptions}}


==Acknowledgements==
==Acknowledgements==

Revision as of 19:31, 18 December 2020

Associate Editor(s)-in-Chief: Henry A. Hoff

"The corepressor complex is recruited to the RNR genes by the sequence-specific DNA-binding protein Crt1, which recognizes the DNA damage response elements (DREs) in the upstream repression sequence (URS) (19, 35)."[1]

Human genes

Consensus sequences

"A consensus sequence, 5'-TAGCCGCCGRRRR-3' (where R = an unspecified purine nucleoside [A/G],was generated from these data."[2]

DNA damage response element (DRE) has the consensus sequence TTTCAAT.[3]

Hypotheses

  1. A1BG has no DNA damage response elements in either promoter.
  2. A1BG is not transcribed by a DNA damage response element.
  3. A DNA damage response element does not participate in the transcription of A1BG.

Samplings

Copying the consensus URS: 5'-TAGCCGCCG-3' and putting the sequence in "⌘F" finds no locations between ZNF497 and A1BG or between ZSCAN22 and A1BG as can be found by the computer programs.

Copying the consensus of the DDRE: 5'-TTTCAAT-3' and putting the sequence in "⌘F" finds no locations for this sequence in any A1BG direction as can be found by the computer programs.

For the Basic programs testing consensus sequence 5'-TTTCAAT-3' (starting with SuccessablesDDRE.bas) written to compare nucleotide sequences with the sequences on either the template strand (-), or coding strand (+), of the DNA, in the negative direction (-), or the positive direction (+), the programs are, are looking for, and found:

  1. negative strand, negative direction, looking for 5'-TTTCAAT-3', 0.
  2. negative strand, positive direction, looking for 5'-TTTCAAT-3', 0.
  3. positive strand, negative direction, looking for 5'-TTTCAAT-3', 0.
  4. positive strand, positive direction, looking for 5'-TTTCAAT-3', 0.
  5. complement, negative strand, negative direction, looking for 5'-AAAGTTA-3', 0.
  6. complement, negative strand, positive direction, looking for 5'-AAAGTTA-3', 0.
  7. complement, positive strand, negative direction, looking for 5'-AAAGTTA-3', 0.
  8. complement, positive strand, positive direction, looking for 5'-AAAGTTA-3', 0.
  9. inverse complement, negative strand, negative direction, looking for 5'-ATTGAAA-3', 0.
  10. inverse complement, negative strand, positive direction, looking for 5'-ATTGAAA-3', 0.
  11. inverse complement, positive strand, negative direction, looking for 5'-ATTGAAA-3', 0.
  12. inverse complement, positive strand, positive direction, looking for 5'-ATTGAAA-3', 0.
  13. inverse negative strand, negative direction, looking for 5'-TAACTTT-3', 0.
  14. inverse negative strand, positive direction, looking for 5'-TAACTTT-3', 0.
  15. inverse positive strand, negative direction, looking for 5'-TAACTTT-3', 0.
  16. inverse positive strand, positive direction, looking for 5'-TAACTTT-3', 0.

Acknowledgements

The content on this page was first contributed by: Henry A. Hoff.

See also

References

  1. Zhengjian Zhang and Joseph C. Reese (17 September 2004). "Redundant Mechanisms Are Used by Ssn6-Tup1 in Repressing Chromosomal Gene Transcription in Saccharomyces cerevisiae". The Journal of Biological Chemistry. 279 (38): 39240–39250. doi:10.1074/jbc.M407159200. PMID 15254041. Retrieved 4 September 2020.
  2. Roberta A. Sumrada and Terrance G. Cooper (June 1987). "Ubiquitous upstream repression sequences control activation of the inducible arginase gene in yeast" (PDF). Proceedings of the National Academy of Sciences USA. 84: 3997–4001. doi:10.1073/pnas.84.12.3997. PMID 3295874. Retrieved 6 September 2020.
  3. Joshua J. Smith, Eric S. Cole, Daniel P. Romero (15 July 2004). "Transcriptional control of RAD51 expression in the ciliate Tetrahymena thermophila". Nucleic Acids Research. 32 (14): 4313–4321. doi:10.1093/nar/gkh771. PMID 15304567. Retrieved 4 September 2020.

External links