Volume 19 Issue 7
Jul.  2021
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ZENG Wei, LIU Yi, LI Wen-ting, LI Yi, ZHU Jin-feng. Bioinformatics analysis of lncRNA DLEU2 transcriptional regulatory factors[J]. Chinese Journal of General Practice, 2021, 19(7): 1114-1116,1120. doi: 10.16766/j.cnki.issn.1674-4152.001998
Citation: ZENG Wei, LIU Yi, LI Wen-ting, LI Yi, ZHU Jin-feng. Bioinformatics analysis of lncRNA DLEU2 transcriptional regulatory factors[J]. Chinese Journal of General Practice, 2021, 19(7): 1114-1116,1120. doi: 10.16766/j.cnki.issn.1674-4152.001998

Bioinformatics analysis of lncRNA DLEU2 transcriptional regulatory factors

doi: 10.16766/j.cnki.issn.1674-4152.001998
Funds:

 2018D01C255

  • Received Date: 2020-06-09
    Available Online: 2022-02-16
  •   Objective  To investigate the structural characteristics of lncRNA DLEU2 transcription factor and its transcriptional binding sites with lncRNA DLEU2.  Methods  Bioinformatics tools were used to analyse the physical and chemical properties, structure, transmembrane region, signal peptide and subcellular localisation of lncRNA DLEU2 transcriptional regulatory factors and to predict the transcriptional binding sites between transcriptional factors and lncRNA DLEU2.  Results  Isoelectric point analysis showed that the isoelectric points of transcriptional regulatory factors CTCF, MAX, ELF1, YY1 and USF1 were less than 7.0. The isoelectric points of POLR2A, FOXA1, BHLHE40, CEBPB and ATF3 were more than 7.0. Lipolysis index analysis showed that the liposolubility index of the above 10 transcriptional regulatory factors were less than 100, indicating that they were hydrophobic proteins. The results of instability index analysis showed that the instability index of 10 transcriptional regulatory factors in this study were greater than 40, indicating that they were unstable proteins. All the secondary structures of the above transcriptional regulatory factors were composed of α-helix, irregular coiling and extended chain structure, and no transmembrane protein and signal peptide structures were found in the above transcriptional factors. Subcellular localisation analysis showed that YY1 was located in the cytoplasm, and other transcription factors were located in the nucleus. At the same time, the 10 transcriptional regulatory factors and lncRNA DLEU2 transcriptional binding sites were predicted.  Conclusion  The diversity of lncRNA DLEU2 transcriptional regulatory factors may contribute to the further study of the regulation of lncRNA DLEU2 transcriptional expression, and the results will be helpful for the screening of lncRNA DLEU2 related cancer therapeutic drugs.

     

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