LINC01209 Gene

Name long intergenic non-protein coding RNA 1209
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nWhile none of the provided abstracts directly address LINC01209, the collective body of work illustrates a range of regulatory mechanisms mediated by key proteins in inflammation, oncogenesis, cell cycle progression, DNA damage response, and tissue differentiation. For example, one study demonstrates that specific NF‑κB pathways are differentially activated through ligand-dependent processing of p100 and subsequent modulation of RelA/p50 versus RelB/p50 complexes, highlighting how alternative pathway components can fine‑tune gene expression in inflammatory and immune responses."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Similarly, research into oncogenic drivers such as metadherin (MTDH) reveals that its interaction with partners like SND1 (also known as Tudor‑SN) is critical for the expansion of tumor‑initiating cells and the progression of cancers, including breast cancer and hepatocellular carcinoma."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional studies further emphasize the multifaceted roles of SND1/Tudor‑SN in regulating cell cycle transitions, mediating transcriptional co‑activation (for instance with factors such as E2F‑1 and PPARγ), and orchestrating DNA repair through interactions with chromatin remodelers and histone acetyltransferases."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "4", "end_ref": "6"}]}, {"type": "t", "text": " In-depth analyses also document the dynamic expression and regulatory impact of SND1 in diverse tissues—in rapidly dividing or progenitor cell populations in contexts from adipogenesis to cardiomyocyte proliferation—as well as its contribution to chromatin relaxation and DNA damage responses."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, in cancer models, the SND1–MTDH complex has been implicated in enhancing tumor growth, metastasis, and therapy resistance, with evidence suggesting that interference in this protein–protein interaction can markedly suppress malignant progression."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "9", "end_ref": "11"}]}, {"type": "t", "text": " Complementary investigations in osteoarthritis and prostate cancer further highlight SND1’s regulatory involvement in inflammatory responses, mitochondrial and extracellular matrix homeostasis, and transcriptional regulation via interaction with other oncogenic transcription factors."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "12", "end_ref": "14"}]}, {"type": "t", "text": " Finally, the control of proliferative responses in vascular smooth muscle cells underscores the broader physiological relevance of these regulatory networks."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "15"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn light of these findings, it is plausible to hypothesize that LINC01209—a long intergenic noncoding RNA not directly discussed in these studies—could participate in similar regulatory networks. Its potential functions might include modulating the assembly or activity of transcriptional complexes, influencing protein–RNA interactions (such as those involving SND1/Tudor‑SN or MTDH), or fine‑tuning signaling pathways that govern cell proliferation, stress responses, and tissue remodeling. Future work is warranted to delineate whether LINC01209 integrates into these established pathways and thereby contributes to the regulation of inflammatory signaling, oncogenesis, or cell cycle progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "14"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Emmanuel Derudder, Emmanuel Dejardin, Linda L Pritchard, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RelB/p50 dimers are differentially regulated by tumor necrosis factor-alpha and lymphotoxin-beta receptor activation: critical roles for p100."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M300106200"}], "href": "https://doi.org/10.1074/jbc.M300106200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12709443"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12709443"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Tekele Fashe, Juha Saarikettu, Pia Isomäki, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Expression analysis of Tudor-SN protein in mouse tissues."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Tissue Cell (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.tice.2012.09.001"}], "href": "https://doi.org/10.1016/j.tice.2012.09.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23068188"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23068188"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Liling Wan, Xin Lu, Salina Yuan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MTDH-SND1 interaction is crucial for expansion and activity of tumor-initiating cells in diverse oncogene- and carcinogen-induced mammary tumors."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Cell (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ccr.2014.04.027"}], "href": "https://doi.org/10.1016/j.ccr.2014.04.027"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24981741"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24981741"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Chao Su, Chunyan Zhang, Adiam Tecle, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Tudor staphylococcal nuclease (Tudor-SN), a novel regulator facilitating G1/S phase transition, acting as a co-activator of E2F-1 in cell cycle regulation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M114.625046"}], "href": "https://doi.org/10.1074/jbc.M114.625046"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25627688"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25627688"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Nidhi Jariwala, Devaraja Rajasekaran, Rachel G Mendoza, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Oncogenic Role of SND1 in Development and Progression of Hepatocellular Carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Res (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/0008-5472.CAN-17-0298"}], "href": "https://doi.org/10.1158/0008-5472.CAN-17-0298"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28428278"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28428278"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Xiao Fu, Chunyan Zhang, Hao Meng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Oncoprotein Tudor-SN is a key determinant providing survival advantage under DNA damaging stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Death Differ (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41418-018-0068-9"}], "href": "https://doi.org/10.1038/s41418-018-0068-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29459768"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29459768"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Xuyang Yao, Mengying Zhai, Lingyi Zhou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Protective effects of SND1 in retinal photoreceptor cell damage induced by ionizing radiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2019.04.189"}], "href": "https://doi.org/10.1016/j.bbrc.2019.04.189"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31084926"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31084926"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Shihu Gan, Chao Su, Jinzheng Ma, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Translation of "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "Tudor-SN"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": ", a novel terminal oligo-pyrimidine (TOP) mRNA, is regulated by the mTORC1 pathway in cardiomyocytes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "RNA Biol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/15476286.2020.1827783"}], "href": "https://doi.org/10.1080/15476286.2020.1827783"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33054526"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33054526"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Minhong Shen, Yong Wei, Hahn Kim, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Small-molecule inhibitors that disrupt the MTDH-SND1 complex suppress breast cancer progression and metastasis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Cancer (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s43018-021-00279-5"}], "href": "https://doi.org/10.1038/s43018-021-00279-5"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35121987"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35121987"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Hanqi Wang, Zhihui Li, Liuping Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "FXR1 impedes the development of osteoarthritis by targeting SND1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Clin Exp Rheumatol (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.55563/clinexprheumatol/2z9o11"}], "href": "https://doi.org/10.55563/clinexprheumatol/2z9o11"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37083155"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37083155"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Lihong Hu, Yufeng Zeng, Lingbiao Xin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SND1, a novel co-activator of HIF1α, promotes tumor initiation in PyMT-induced breast tumor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS J (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/febs.16940"}], "href": "https://doi.org/10.1111/febs.16940"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37622244"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37622244"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Shufeng Lin, Huiyang Guo, Xiaoxuan You, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SND1 aggravates mitochondrial damage, apoptosis and extracellular matrix degradation in IL-1β-stimulated chondrocytes via PINK1/BECN1 pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Med Res (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s40001-023-01340-y"}], "href": "https://doi.org/10.1186/s40001-023-01340-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37749650"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37749650"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Tanner Wright, Yalong Wang, Sabrina A Stratton, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Loss of the methylarginine reader function of SND1 confers resistance to hepatocellular carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem J (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1042/BCJ20230384"}], "href": "https://doi.org/10.1042/BCJ20230384"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37905668"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37905668"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Sheng-You Liao, Dmytro Rudoy, Sander B Frank, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SND1 binds to ERG and promotes tumor growth in genetic mouse models of prostate cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-023-43245-8"}], "href": "https://doi.org/10.1038/s41467-023-43245-8"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37973913"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37973913"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Chao Su, Mingxia Liu, Xuyang Yao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Vascular injury activates the ELK1/SND1/SRF pathway to promote vascular smooth muscle cell proliferative phenotype and neointimal hyperplasia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Mol Life Sci (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00018-023-05095-x"}], "href": "https://doi.org/10.1007/s00018-023-05095-x"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38279051"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38279051"}]}]}]}
NCBI Gene ID 101928684
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Predicted Functions View LINC01209's ARCHS4 Predicted Functions.
Co-expressed Genes View LINC01209's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View LINC01209's ARCHS4 Predicted Functions.

Functional Associations

LINC01209 has 1 functional associations with biological entities spanning 1 categories (gene, protein or microRNA) extracted from 1 datasets.

Click the + buttons to view associations for LINC01209 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
GEO Signatures of Differentially Expressed Genes for Kinase Perturbations kinase perturbations changing expression of LINC01209 gene from the GEO Signatures of Differentially Expressed Genes for Kinase Perturbations dataset.