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==Literature Characterization==
 
==Literature Characterization==
 
The study made an analysis of the site of transcription initiation, which was driven by the U6 promoter.
 
The study made an analysis of the site of transcription initiation, which was driven by the U6 promoter.
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"src="https://static.igem.wiki/teams/4586/wiki/literature-characterisation-parts/u6-promoter.png">
 
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lang=EN style='font-size:11.0pt;line-height:115%'>T(a) Here we have the transcription initiation site for sh1005 serial mutations. The nucleotides that replace the A in position -1 of sh1005 are identified by lowercase letters. and in boxes we have the presumed initiation site of transcription. The red mark is the real initiation site; the bold mark The original SH1005 (b) They made the dual-luciferase assay to assess the functionality of sh1005 serial mutations. (c) The transcription initiation site for small RNAs (~21 nt in length), in which the nucleotides around the initiation site are different. nucleotides added between the -2 position of the U6 promoter and the universal sequence GATAATTTGTGGTAGTGGTT are referred to by lowercase letters. Asterisks are used to assess constructs for which an insufficient number of reads were sequenced to indicate the exact initiation site. (d) transcription initiation is affected by the sequence upstream of the -1 site. Red mark The initiation sites of the indicated sh1005 mutations with changed sequences upstream of the -1 siteز
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lang=EN style='font-size:11.0pt;line-height:115%'>(a) Here we have the transcription initiation site for sh1005 serial mutations. The nucleotides that replace the A in position -1 of sh1005 are identified by lowercase letters. and in boxes we have the presumed initiation site of transcription. The red mark is the real initiation site; the bold mark The original SH1005 (b) They made the dual-luciferase assay to assess the functionality of sh1005 serial mutations. (c) The transcription initiation site for small RNAs (~21 nt in length), in which the nucleotides around the initiation site are different. nucleotides added between the -2 position of the U6 promoter and the universal sequence GATAATTTGTGGTAGTGGTT are referred to by lowercase letters. Asterisks are used to assess constructs for which an insufficient number of reads were sequenced to indicate the exact initiation site. (d) transcription initiation is affected by the sequence upstream of the -1 site. Red mark The initiation sites of the indicated sh1005 mutations with changed sequences upstream of the -1 siteز
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==Experimental Characterization==
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In order to amplify this DNA part, we used PCR amplification to reach the desired concentration to complete our experiments using specific forward and reverse primers, running the parts on gel electrophoresis as this part presents in lane (P7) including Guide RNA and Human U6 promoter, and then measuring the specific concentration of the running part using Real-Time PCR as shown in the following figure.
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We performed the double digestion method for this part in the prefix and suffix with its specific restriction enzyme and applied this part to gel electrophoresis as shown in the following figure lane (P7).
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===Usage and Biology===
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===Functional Parameters===
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==References==
 
==References==

Latest revision as of 20:55, 11 October 2023


Human U6 promoter

Part Description

It is a type III RNA polymerase III promoter that controls the expression of short RNAs. Distance sequence element (DSE), proximal sequence element (PSE), and TATA box are the three primary components of the U6 promoter. The nucleotide G indicates the U6 promoter's transcriptional beginning location.

Usage

It is a promoter that controls the production of the guide RNA that directs Cas12k to the target.

Literature Characterization

The study made an analysis of the site of transcription initiation, which was driven by the U6 promoter.

(a) Here we have the transcription initiation site for sh1005 serial mutations. The nucleotides that replace the A in position -1 of sh1005 are identified by lowercase letters. and in boxes we have the presumed initiation site of transcription. The red mark is the real initiation site; the bold mark The original SH1005 (b) They made the dual-luciferase assay to assess the functionality of sh1005 serial mutations. (c) The transcription initiation site for small RNAs (~21 nt in length), in which the nucleotides around the initiation site are different. nucleotides added between the -2 position of the U6 promoter and the universal sequence GATAATTTGTGGTAGTGGTT are referred to by lowercase letters. Asterisks are used to assess constructs for which an insufficient number of reads were sequenced to indicate the exact initiation site. (d) transcription initiation is affected by the sequence upstream of the -1 site. Red mark The initiation sites of the indicated sh1005 mutations with changed sequences upstream of the -1 siteز

Experimental Characterization

In order to amplify this DNA part, we used PCR amplification to reach the desired concentration to complete our experiments using specific forward and reverse primers, running the parts on gel electrophoresis as this part presents in lane (P7) including Guide RNA and Human U6 promoter, and then measuring the specific concentration of the running part using Real-Time PCR as shown in the following figure.





We performed the double digestion method for this part in the prefix and suffix with its specific restriction enzyme and applied this part to gel electrophoresis as shown in the following figure lane (P7).


References

Ma, H., Wu, Y., Dang, Y., Choi, J. G., Zhang, J., & Wu, H. (2014). Pol III promoters to express small RNAs: delineation of transcription initiation. Molecular Therapy-Nucleic Acids, 3. Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]