User:Marshallsumter: Difference between revisions

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==Human genes==
==Human genes==
{{main|Human genes}}
 


==Gene expressions==
==Gene expressions==
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==Interactions==
==Interactions==
{{main|Interaction gene transcriptions}}
 


==Consensus sequences==
==Consensus sequences==
{{main|Consensus sequence gene transcriptions}}
 


==Binding site for==
==Binding site for==
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==Complement-inverse copies==
==Complement-inverse copies==
{{main|Complement-inverse copy gene transcriptions}}
 


==Enhancer activity==
==Enhancer activity==
{{main|Enhancer activity copy gene transcriptions}}
 


==Promoter occurrences==
==Promoter occurrences==
{{main|Promoter occurrence gene transcriptions}}
 


==Hypotheses==
==Hypotheses==
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===RDr alternate positive direction (evens) (4050-1) distal promoters===
===RDr alternate positive direction (evens) (4050-1) distal promoters===


==DCE SIII analysis and results==
==Response element analysis and results==
{{main|Complex locus A1BG and ZNF497#DCESIII}}
{{main|Complex locus A1BG and ZNF497#Name of response elements}}
The consensus sequence for the DCE is CTTC...CTGT...AGC.<ref name=Lee/> These three consensus elements are referred to as subelements: "S<sub>I</sub> is CTTC, S<sub>II</sub> is CTGT, and S<sub>III</sub> is AGC."<ref name=Lee/>
The Pax-4 homeodomain [HD] was shown to preferentially dimerize on DNA sequences consisting of an inverted TAAT motif, separated by 4-nucleotide spacing."<ref name=Kalousova/>


{|class="wikitable"
{|class="wikitable"
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! Reals or randoms !! Promoters !! direction !! Numbers !! Strands !! Occurrences !! Averages (± 0.1)  
! Reals or randoms !! Promoters !! direction !! Numbers !! Strands !! Occurrences !! Averages (± 0.1)  
|-
|-
| Reals || UTR || negative || 79 || 2 || 39.5 || 0  
| Reals || UTR || negative || 0 || 2 || 0 || 0  
|-
|-
| Randoms || UTR || arbitrary negative || 0 || 10 || 0 || 0  
| Randoms || UTR || arbitrary negative || 0 || 10 || 0 || 0  
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| Randoms || Core || alternate negative || 0 || 10 || 0 || 0  
| Randoms || Core || alternate negative || 0 || 10 || 0 || 0  
|-
|-
| Reals || Core || positive || 9 || 2 || 4.5 || 4.5 ± (-+6,++3)
| Reals || Core || positive || 0 || 2 || 0 || 0
|-
|-
| Randoms || Core || arbitrary positive || 0 || 10 || 0 || 0
| Randoms || Core || arbitrary positive || 0 || 10 || 0 || 0
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| Randoms || Core || alternate positive || 0 || 10 || 0 || 0  
| Randoms || Core || alternate positive || 0 || 10 || 0 || 0  
|-
|-
| Reals || Proximal || negative || 10 || 2 || 5 || 5
| Reals || Proximal || negative || 0 || 2 || 0 || 0
|-
|-
| Randoms || Proximal || arbitrary negative || 0 || 10 || 0 || 0  
| Randoms || Proximal || arbitrary negative || 0 || 10 || 0 || 0  
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| Randoms || Proximal || alternate negative || 0 || 10 || 0 || 0  
| Randoms || Proximal || alternate negative || 0 || 10 || 0 || 0  
|-
|-
| Reals || Proximal || positive || 3 || 2 || 1.5 || 1.5 ± (-2,++1)
| Reals || Proximal || positive || 0 || 2 || 0 || 0
|-
|-
| Randoms || Proximal || arbitrary positive || 0 || 10 || 0 || 0  
| Randoms || Proximal || arbitrary positive || 0 || 10 || 0 || 0  
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| Randoms || Proximal || alternate positive || 0 || 10 || 0 || 0  
| Randoms || Proximal || alternate positive || 0 || 10 || 0 || 0  
|-
|-
| Reals || Distal || negative || 115 || 2 || 57.5 || 57.5 ± 22.5 (--25,+-90)
| Reals || Distal || negative || 0 || 2 || 0 || 0
|-
|-
| Randoms || Distal || arbitrary negative || 0 || 10 || 0 || 0
| Randoms || Distal || arbitrary negative || 0 || 10 || 0 || 0
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| Randoms || Distal || alternate negative || 0 || 10 || 0 || 0  
| Randoms || Distal || alternate negative || 0 || 10 || 0 || 0  
|-
|-
| Reals || Distal || positive || 253 || 2 || 126.5 || 126.5 ± 65.5 (-+192,61++)
| Reals || Distal || positive || 0 || 2 || 0 || 0
|-
|-
| Randoms || Distal || arbitrary positive || 0 || 10 || 0 || 0  
| Randoms || Distal || arbitrary positive || 0 || 10 || 0 || 0  
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Comparison:
Comparison:


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


==Acknowledgements==
==Acknowledgements==

Revision as of 20:42, 26 December 2022

Editor-In-Chief: Henry A. Hoff

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

Human genes

Gene expressions

Main article: Gene expressions

Interactions

Consensus sequences

Binding site for

Complement copies

Main article: Complement copy gene transcriptions

Inverse copies

Main article: Inverse copy gene transcriptions

Complement-inverse copies

Enhancer activity

Promoter occurrences

Hypotheses

Main article: Hypotheses
  1. A1BG has no regulatory elements in either promoter.
  2. A1BG is not transcribed by a regulatory element.
  3. No regulatory element participates in the transcription of A1BG.

Response element samplings

Copying a responsive elements consensus sequence AAAAAAAA and putting the sequence in "⌘F" finds none between ZNF497 and A1BG or none between ZSCAN22 and A1BG as can be found by the computer programs.

For the Basic programs testing consensus sequence AAAAAAAA (starting with SuccessablesAAA.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 AAAAAAAA, 0.
  2. positive strand, negative direction, looking for AAAAAAAA, 0.
  3. negative strand, positive direction, looking for AAAAAAAA, 0.
  4. positive strand, positive direction, looking for AAAAAAAA, 0.
  5. inverse complement, negative strand, negative direction, looking for TTTTTTTT, 0.
  6. inverse complement, positive strand, negative direction, looking for TTTTTTTT, 0.
  7. inverse complement, negative strand, positive direction, looking for TTTTTTTT, 0.
  8. inverse complement, positive strand, positive direction, looking for TTTTTTTT, 0.

AAA (4560-2846) UTRs

AAA negative direction (2846-2811) core promoters

AAA positive direction (4445-4265) core promoters

AAA negative direction (2811-2596) proximal promoters

AAA positive direction (4265-4050) proximal promoters

AAA negative direction (2596-1) distal promoters

AAA positive direction (4050-1) distal promoters

Response element 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 arbitrary (evens) (4560-2846) UTRs

RDr alternate (odds) (4560-2846) UTRs

RDr arbitrary negative direction (evens) (2846-2811) core promoters

RDr alternate negative direction (odds) (2846-2811) core promoters

RDr arbitrary positive direction (odds) (4445-4265) core promoters

RDr alternate positive direction (evens) (4445-4265) core promoters

RDr arbitrary negative direction (evens) (2811-2596) proximal promoters

RDr alternate negative direction (odds) (2811-2596) proximal promoters

RDr arbitrary positive direction (odds) (4265-4050) proximal promoters

RDr alternate positive direction (evens) (4265-4050) proximal promoters

RDr arbitrary negative direction (evens) (2596-1) distal promoters

RDr alternate negative direction (odds) (2596-1) distal promoters

RDr arbitrary positive direction (odds) (4050-1) distal promoters

RDr alternate positive direction (evens) (4050-1) distal promoters

Response element analysis and results

Main article: Complex locus A1BG and ZNF497 § Name of response elements

The Pax-4 homeodomain [HD] was shown to preferentially dimerize on DNA sequences consisting of an inverted TAAT motif, separated by 4-nucleotide spacing."[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 arbitrary negative 0 10 0 0
Randoms Core alternate negative 0 10 0 0
Reals Core positive 0 2 0 0
Randoms Core arbitrary positive 0 10 0 0
Randoms Core alternate positive 0 10 0 0
Reals Proximal negative 0 2 0 0
Randoms Proximal arbitrary negative 0 10 0 0
Randoms Proximal alternate negative 0 10 0 0
Reals Proximal positive 0 2 0 0
Randoms Proximal arbitrary positive 0 10 0 0
Randoms Proximal alternate positive 0 10 0 0
Reals Distal negative 0 2 0 0
Randoms Distal arbitrary negative 0 10 0 0
Randoms Distal alternate negative 0 10 0 0
Reals Distal positive 0 2 0 0
Randoms Distal arbitrary positive 0 10 0 0
Randoms Distal alternate positive 0 10 0 0

Comparison:

The occurrences of real responsive element consensus sequences are greater 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.

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

Initial content for this page in some instances incorporates text from the United States National Library of Medicine.

See also

References

  1. ↑

External links

{{Phosphate biochemistry}}


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