| HGNC Family | Non-coding RNAs |
| Name | microRNA 1305 |
| Description | microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe diverse regulatory roles of miR‑1305 have been demonstrated in the differentiation of mesenchymal stem cells. In human synovium‑derived MSCs, lncRNA DANCR promotes chondrogenesis by down‑regulating miR‑1305, and forced expression of miR‑1305 counteracts DANCR‑induced cell proliferation and chondrogenic differentiation through modulation of the TGF‑β pathway member Smad4."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Similarly, during osteogenic differentiation of human MSCs, the circular RNA circ_0076906 functions as a molecular sponge for miR‑1305, thereby controlling the expression of its target gene Osteoglycin (OGN) and promoting bone formation to alleviate osteoporosis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn human pluripotent stem cells, including embryonic and induced pluripotent stem cells, miR‑1305 has emerged as a crucial regulator of cell fate. Its expression levels vary with cell cycle progression, where miR‑1305 overexpression induces differentiation, accelerates the G1/S transition, and increases apoptosis by targeting the transcription factor POLR3G. Conversely, down‑regulation of miR‑1305 helps maintain pluripotency and enhances cell survival."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurthermore, in the context of cervical squamous cell carcinoma, miR‑1305 exhibits tumor‑suppressive properties. Here, a different circular RNA, circ_0072008, acts as a sponge for miR‑1305; the consequent reduction in miR‑1305 activity leads to increased expression of HELLS, a helicase linked to enhanced cell proliferation, migration, and invasion. These findings highlight the potential of targeting the miR‑1305/HELLS axis for therapeutic interventions in cervical cancer."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Lei Zhang, Xiangyi Sun, Shuo Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long noncoding RNA DANCR regulates "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "miR-1305"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": "-Smad 4 axis to promote chondrogenic differentiation of human synovium-derived mesenchymal stem cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biosci Rep (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1042/BSR20170347"}], "href": "https://doi.org/10.1042/BSR20170347"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28674107"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28674107"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Jian Wen, Zhiping Guan, Binsheng Yu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circular RNA hsa_circ_0076906 competes with OGN for miR-1305 biding site to alleviate the progression of osteoporosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Biochem Cell Biol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biocel.2020.105719"}], "href": "https://doi.org/10.1016/j.biocel.2020.105719"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32087327"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32087327"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Shibo Jin, Joseph Collin, Lili Zhu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A Novel Role for miR-1305 in Regulation of Pluripotency-Differentiation Balance, Cell Cycle, and Apoptosis in Human Pluripotent Stem Cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Stem Cells (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/stem.2444"}], "href": "https://doi.org/10.1002/stem.2444"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27339422"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27339422"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Chunhua He, Leng Liu "}, {"type": "b", "children": [{"type": "t", "text": "Hsa_circ_0072008 regulates cell proliferation, migration, and invasion in cervical squamous cell carcinoma via miR-1305/helicase, lymphoid specific (HELLS) axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Bioengineered (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21655979.2022.2048945"}], "href": "https://doi.org/10.1080/21655979.2022.2048945"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35311456"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35311456"}]}]}]}
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| Synonyms | MIRN1305, HSA-MIR-1305, MIR-1305 |
| NCBI Gene ID | 100302270 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR1305 has 206 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 11 datasets.
Click the + buttons to view associations for MIR1305 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR1305 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR1305 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of MIR1305 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR1305 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR1305 gene from the ENCODE Histone Modification Site Profiles dataset. | |
| ENCODE Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR1305 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR1305 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR1305 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR1305 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of MIR1305 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR1305 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |