H and ACA box gene transcriptions: Difference between revisions

Jump to navigation Jump to search
Line 59: Line 59:
# inverse, positive strand, negative direction, is SuccessablesHACAi+-.bas, looking for 5'-AGGACA-3', 3, 5'-AGGACA-3' at 3389, 5'-AGGACA-3' at 3756, 5'-AGGACA-3' at 4468.
# inverse, positive strand, negative direction, is SuccessablesHACAi+-.bas, looking for 5'-AGGACA-3', 3, 5'-AGGACA-3' at 3389, 5'-AGGACA-3' at 3756, 5'-AGGACA-3' at 4468.
# inverse, positive strand, positive direction, is SuccessablesHACAi++.bas, looking for 5'-AGGACA-3', 2, 5'-AGGACA-3' at 144, 5'-AGGACA-3' at 3622.
# inverse, positive strand, positive direction, is SuccessablesHACAi++.bas, looking for 5'-AGGACA-3', 2, 5'-AGGACA-3' at 144, 5'-AGGACA-3' at 3622.
===AAA UTRs===
{{main|UTR promoter gene transcriptions}}
===AAA core promoters===
{{main|Core promoter gene transcriptions}}
===AAA proximal promoters===
{{main|Proximal promoter gene transcriptions}}
===AAA distal promoters===
{{main|Distal promoter gene transcriptions}}
==Random dataset samplings==
# RDr0: 0.
# RDr1: 0.
# RDr2: 0.
# RDr3: 0.
# RDr4: 0.
# RDr5: 0.
# RDr6: 0.
# RDr7: 0.
# RDr8: 0.
# RDr9: 0.
# RDr0ci: 0.
# RDr1ci: 0.
# RDr2ci: 0.
# RDr3ci: 0.
# RDr4ci: 0.
# RDr5ci: 0.
# RDr6ci: 0.
# RDr7ci: 0.
# RDr8ci: 0.
# RDr9ci: 0.
===RDr UTRs===
===RDr core promoters===
===RDr proximal promoters===
===RDr distal promoters===
==Response element analysis and results==
{{main|Complex locus A1BG and ZNF497#H and ACA boxes}}
The combined consensus sequence is 5'-ACAGGA-3'.<ref name=Mitchell/>
{|class="wikitable"
|-
! Reals or randoms !! Promoters !! direction !! Numbers !! Strands !! Occurrences !! Averages (± 0.1)
|-
| Reals || UTR || negative || 0 || 2 || 0 || 0
|-
| Randoms || UTR || arbitrary negative || 0 || 10 || 0 || 0
|-
| Randoms || UTR || alternate negative || 0 || 10 || 0 || 0
|-
| Reals || Core || negative || 0 || 2 || 0 || 0
|-
| Randoms || Core || negative || 0 || 10 || 0 || 0
|-
| Reals || Core || positive || 0 || 2 || 0 || 0
|-
| Randoms || Core || positive || 0 || 10 || 0 || 0
|-
| Reals || Proximal || negative || 0 || 2 || 0 || 0
|-
| Randoms || Proximal || negative || 0 || 10 || 0 || 0
|-
| Reals || Proximal || positive || 0 || 2 || 0 || 0
|-
| Randoms || Proximal || positive || 0 || 10 || 0 || 0
|-
| Reals || Distal || negative || 0 || 2 || 0 || 0
|-
| Randoms || Distal || negative || 0 || 10 || 0 || 0
|-
| Reals || Distal || positive || 0 || 2 || 0 || 0
|-
| Randoms || Distal || positive || 0 || 10 || 0 || 0
|}
Comparison:
The occurrences of real responsive element consensus sequences are larger than the randoms. This suggests that the real responsive element consensus sequences are likely active or activable.


==Acknowledgements==
==Acknowledgements==

Revision as of 06:08, 30 April 2022

Editor-In-Chief: Henry A. Hoff

Consensus sequences

"The box H/ACA snoRNAs were most recently recognized as a small RNA family by virtue of an ACA trinucleotide located 3 nt upstream of the mature snoRNA 3' end (41). In addition to this ACA box, they have the consensus H box sequence (5'-ANANNA-3') but have no other primary sequence identity. Despite this lack of primary sequence conservation, the H and ACA boxes are embedded in an evolutionarily conserved hairpin-hinge-hairpin-tail core secondary structure with the H box in the single-stranded hinge region and the ACA box in the single-stranded tail (5, 16)."[1]

The "3' end of mature hTR (45) has an ACA trinucleotide 3 nt upstream of its 3' end. In addition, the 3' region of hTR contains a single H box consensus sequence (5'-AGAGGA-3')."[1]

"Comparison with the murine telomerase RNA (mTR) (7) suggests that the snoRNA-like features of hTR are evolutionarily conserved. The mTR 3' end (nt 169 to 397 as numbered in reference 25) has ~76% sequence identity with the corresponding region of hTR (nt 211 to 451) and includes consensus H (5'-ACAGGA-3') and ACA box sequences."[1]

An H box has a consensus sequence of 3'-ACACCA-5'.[2]

The combined consensus sequence is 5'-ACAGGA-3'.[1]

H and ACA boxes in promoters of A1BG

For the Basic programs (starting with SuccessablesHACA.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 is SuccessablesHACA--.bas, looking for 5'-ACAGGA-3', 0.
  2. negative strand, positive direction is SuccessablesHACA-+.bas, looking for 5'-ACAGGA-3', 1, 5'-ACAGGA-3' at 3572.
  3. positive strand, negative direction is SuccessablesHACA+-.bas, looking for 5'-ACAGGA-3', 1, 5'-ACAGGA-3' at 2690.
  4. positive strand, positive direction is SuccessablesHACA++.bas, looking for 5'-ACAGGA-3', 1, 5'-ACAGGA-3' at 3620.
  5. complement, negative strand, negative direction is SuccessablesHACAc--.bas, looking for 5'-TGTCCT-3', 1, 5'-TGTCCT-3' at 2690.
  6. complement, negative strand, positive direction is SuccessablesHACAc-+.bas, looking for 5'-TGTCCT-3', 1, 5'-TGTCCT-3' at 3620.
  7. complement, positive strand, negative direction is SuccessablesHACAc+-.bas, looking for 5'-TGTCCT-3', 0.
  8. complement, positive strand, positive direction is SuccessablesHACAc++.bas, looking for 5'-TGTCCT-3', 1, 5'-TGTCCT-3' at 3572.
  9. inverse complement, negative strand, negative direction is SuccessablesHACAci--.bas, looking for 5'-TCCTGT-3', 3, 5'-TCCTGT-3' at 3389, 5'-TCCTGT-3' at 3756, 5'-TCCTGT-3' at 4468.
  10. inverse complement, negative strand, positive direction is SuccessablesHACAci-+.bas, looking for 5'-TCCTGT-3', 2, 5'-TCCTGT-3' at 144, 5'-TCCTGT-3' at 3622.
  11. inverse complement, positive strand, negative direction is SuccessablesHACAci+-.bas, looking for 5'-TCCTGT-3', 1, 5'-TCCTGT-3' at 1911.
  12. inverse complement, positive strand, positive direction is SuccessablesHACAci++.bas, looking for 5'-TCCTGT-3', 3, 5'-TCCTGT-3' at 2460, 5'-TCCTGT-3' at 3131, 5'-TCCTGT-3' at 4252.
  13. inverse, negative strand, negative direction, is SuccessablesHACAi--.bas, looking for 5'-AGGACA-3', 1, 5'-AGGACA-3' at 1911.
  14. inverse, negative strand, positive direction, is SuccessablesHACAi-+.bas, looking for 5'-AGGACA-3', 3, 3'-AGGACA-3' at 2460, 3'-AGGACA-3' at 3131, 3'-AGGACA-3' at 4252.
  15. inverse, positive strand, negative direction, is SuccessablesHACAi+-.bas, looking for 5'-AGGACA-3', 3, 5'-AGGACA-3' at 3389, 5'-AGGACA-3' at 3756, 5'-AGGACA-3' at 4468.
  16. inverse, positive strand, positive direction, is SuccessablesHACAi++.bas, looking for 5'-AGGACA-3', 2, 5'-AGGACA-3' at 144, 5'-AGGACA-3' at 3622.

AAA UTRs

AAA core promoters

AAA proximal promoters

AAA distal promoters

Random dataset samplings

  1. RDr0: 0.
  2. RDr1: 0.
  3. RDr2: 0.
  4. RDr3: 0.
  5. RDr4: 0.
  6. RDr5: 0.
  7. RDr6: 0.
  8. RDr7: 0.
  9. RDr8: 0.
  10. RDr9: 0.
  11. RDr0ci: 0.
  12. RDr1ci: 0.
  13. RDr2ci: 0.
  14. RDr3ci: 0.
  15. RDr4ci: 0.
  16. RDr5ci: 0.
  17. RDr6ci: 0.
  18. RDr7ci: 0.
  19. RDr8ci: 0.
  20. RDr9ci: 0.

RDr UTRs

RDr core promoters

RDr proximal promoters

RDr distal promoters

Response element analysis and results

The combined consensus sequence is 5'-ACAGGA-3'.[1]

Reals or randoms Promoters direction Numbers Strands Occurrences Averages (± 0.1)
Reals UTR negative 0 2 0 0
Randoms UTR arbitrary negative 0 10 0 0
Randoms UTR alternate negative 0 10 0 0
Reals Core negative 0 2 0 0
Randoms Core negative 0 10 0 0
Reals Core positive 0 2 0 0
Randoms Core positive 0 10 0 0
Reals Proximal negative 0 2 0 0
Randoms Proximal negative 0 10 0 0
Reals Proximal positive 0 2 0 0
Randoms Proximal positive 0 10 0 0
Reals Distal negative 0 2 0 0
Randoms Distal negative 0 10 0 0
Reals Distal positive 0 2 0 0
Randoms Distal positive 0 10 0 0

Comparison:

The occurrences of real responsive element consensus sequences are larger than the randoms. This suggests that the real responsive element consensus sequences are likely active or activable.

Acknowledgements

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

Initial content for this page in some instances came from Wikiversity.

See also

References

  1. 1.0 1.1 1.2 1.3 1.4 James R. Mitchell, Jeffrey Cheng, ang Kathleen Collins (January 1999). "A Box H/ACA Small Nucleolar RNA-Like Domain at the Human Telomerase RNA 3' End" (PDF). Molecular and Cellular Biology. 19 (1): 567–576. Retrieved 5 November 2018.
  2. Timofey S. Rozhdestvensky, Thean Hock Tang, Inna V. Tchirkova, Jürgen Brosius, Jean‐Pierre Bachellerie and Alexander Hüttenhofer (2003). "Binding of L7Ae protein to the K‐turn of archaeal snoRNAs: a shared RNA binding motif for C/D and H/ACA box snoRNAs in Archaea". Nucleic Acids Research. 31 (3): 869–77. doi:10.1093/nar/gkg175. Retrieved 2014-06-08.

External links

Template:Sisterlinks