Difference between revisions of "Part:BBa K4789007"
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[3]Zhang Xian-Yu,Ma Huan,Li Jing et al. Functional implications of miR-145/RCAN3 axis in the progression of cervical cancer.[J] .Reprod Biol, 2020, 20: 140-146. | [3]Zhang Xian-Yu,Ma Huan,Li Jing et al. Functional implications of miR-145/RCAN3 axis in the progression of cervical cancer.[J] .Reprod Biol, 2020, 20: 140-146. | ||
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+ | [4]Han Xiting,Wang Qian,Wang Yan et al. Long non-coding RNA metastasis-associated lung adenocarcinoma transcript 1/microRNA-202-3p/periostin axis modulates invasion and epithelial-mesenchymal transition in human cervical cancer.[J] .J Cell Physiol, 2019, 234: 14170-14180. | ||
[5] http://www.mircode.org/ | [5] http://www.mircode.org/ |
Latest revision as of 07:54, 30 September 2023
pcDNA-pre-miR-145
Usage and Biology
MicroRNAs (miRNAs), a novelty-defined class of regulatory genes, have revolutionized principles of classical bimolecular. These RNAs regulate the expression of a gene through inhibition of translational initiation or targeting mRNAs for degradation. MiR-145 has the diagnose value in patients with cervical cancer[1].Our team also focus on the cervical cancer screening. Previous researches have discovered miR-145 could inhibit cervical cancer progression through targeting WNT2B by Wnt/β-catenin pathway[2] or miR-145/RCAN3 axis[3] and so on. LncRNAs work as ‘miRNA sponges’ through binding to specific miRNAs. Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), long non-coding RNA, has been reported to be upregulated in cervical cancer tissues and promote cancer cell invasion and metastasis[4]. Pre-mir-145 could bind to the sequence of MALAT1 according to the prediction database miRcode(Figure 1)[5]. This mechanism gives rise to our idea about fusing a sponge RNA based on the sequences of lncRNA with binding sites complementary to the sequence of miRNA into a plasmid contained the reporter gene. In our study, we cloned the pre-miR145 sequence into the basic part pcDNA 3.0 plasmid. Then the miR22 could overexpressed in the Hela cell.
Figure 1 miR-145and LncRNA binding site
Reference
[1]Yu Furong,Liu Jie,Dong Weilei et al. The diagnostic value of miR-145 and miR-205 in patients with cervical cancer.[J] .Am J Transl Res, 2021, 13: 1825-1832.
[2 ]Li Qi,Yu Xiaohong,Yang Liangliang,MiR-145 inhibits cervical cancer progression and metastasis by targeting WNT2B by Wnt/β-catenin pathway.[J] .Int J Clin Exp Pathol, 2019, 12: 3740-3751.
[3]Zhang Xian-Yu,Ma Huan,Li Jing et al. Functional implications of miR-145/RCAN3 axis in the progression of cervical cancer.[J] .Reprod Biol, 2020, 20: 140-146.
[4]Han Xiting,Wang Qian,Wang Yan et al. Long non-coding RNA metastasis-associated lung adenocarcinoma transcript 1/microRNA-202-3p/periostin axis modulates invasion and epithelial-mesenchymal transition in human cervical cancer.[J] .J Cell Physiol, 2019, 234: 14170-14180.
[5] http://www.mircode.org/
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 952
Illegal XbaI site found at 991
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Illegal SpeI site found at 935
Illegal PstI site found at 957
Illegal PstI site found at 2313 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 952
Illegal NheI site found at 895
Illegal SpeI site found at 249
Illegal SpeI site found at 935
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Illegal PstI site found at 2313
Illegal NotI site found at 978 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 952
Illegal BglII site found at 12
Illegal BamHI site found at 929
Illegal XhoI site found at 985 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 952
Illegal XbaI site found at 991
Illegal SpeI site found at 249
Illegal SpeI site found at 935
Illegal PstI site found at 957
Illegal PstI site found at 2313 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 952
Illegal XbaI site found at 991
Illegal SpeI site found at 249
Illegal SpeI site found at 935
Illegal PstI site found at 957
Illegal PstI site found at 2313
Illegal NgoMIV site found at 1423
Illegal NgoMIV site found at 2764
Illegal NgoMIV site found at 3047 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 882
Illegal BsaI.rc site found at 4572
Illegal SapI site found at 3492
Illegal SapI.rc site found at 2613
Illegal SapI.rc site found at 2823