MIR378J Gene

HGNC Family Non-coding RNAs
Name microRNA 378j
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": "\nAlthough the query mentioned MIR378J, the provided abstracts do not discuss this microRNA. Instead, they focus on the multifunctional roles of syntaxin 17 (STX17), a SNARE protein that is essential for several cellular degradation and quality‐control pathways. STX17 is selectively recruited to completed autophagosomes—facilitated by its unique C-terminal hairpin and interactions with SNAP29 and various vesicle‐targeting SNAREs—to mediate their fusion with late endosomes or lysosomes, ensuring efficient cargo degradation and mitochondrial quality control via mitophagy."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n \nFurthermore, STX17 functions extend beyond conventional autophagy. It plays a key role in processes such as mitochondrial-derived vesicle trafficking under stress conditions and in the cellular response to infection. For example, during microbial invasion, bacterial effectors may cleave STX17 to simultaneously block autophagy and apoptosis, thereby disrupting mitochondrial dynamics and immune signaling. STX17’s involvement in neuronal injury following ischemia/reperfusion and its localization at mitochondria-associated endoplasmic reticulum membranes also underscore its importance in maintaining cellular homeostasis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "3", "end_ref": "5"}]}, {"type": "t", "text": "\n \nMoreover, modulation of STX17—in terms of its expression and stability—is implicated in several pathophysiological contexts. Studies describe how upregulation of regulatory non-coding RNAs (such as lncRNA-GAS5) can promote the degradation of STX17, leading to impaired autophagic flux and heightened inflammatory responses during bacterial infection, while its depletion in neurons aggravates toxin-induced damage. In addition, interactions between STX17 and innate immune regulators like STING further integrate energy stress signals with autophagy, thereby influencing exercise endurance, glucose metabolism, and neurotoxicity outcomes."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "6", "end_ref": "8"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Eisuke Itakura, Chieko Kishi-Itakura, Noboru Mizushima "}, {"type": "b", "children": [{"type": "t", "text": "The hairpin-type tail-anchored SNARE syntaxin 17 targets to autophagosomes for fusion with endosomes/lysosomes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.cell.2012.11.001"}], "href": "https://doi.org/10.1016/j.cell.2012.11.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23217709"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23217709"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Gian-Luca McLelland, Sydney A Lee, Heidi M McBride, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Syntaxin-17 delivers PINK1/parkin-dependent mitochondrial vesicles to the endolysosomal system."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.201603105"}], "href": "https://doi.org/10.1083/jcb.201603105"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27458136"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27458136"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Kohei Arasaki, Yumi Mikami, Stephanie R Shames, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Legionella effector Lpg1137 shuts down ER-mitochondria communication through cleavage of syntaxin 17."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncomms15406"}], "href": "https://doi.org/10.1038/ncomms15406"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28504273"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28504273"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Lei Chen, Yun-Fei Xia, Shu-Fang Shen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Syntaxin 17 inhibits ischemic neuronal injury by resuming autophagy flux and ameliorating endoplasmic reticulum stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Free Radic Biol Med (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.freeradbiomed.2020.08.010"}], "href": "https://doi.org/10.1016/j.freeradbiomed.2020.08.010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32828953"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32828953"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Haixia Xu, Wenjun Yu, Mingming Sun, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Syntaxin17 contributes to obesity cardiomyopathy through promoting mitochondrial Ca"}, {"type": "a", "children": [{"type": "t", "text": "sup"}], "href": "sup"}, {"type": "t", "text": "2+"}, {"type": "a", "children": [{"type": "t", "text": "/sup"}], "href": "/sup"}, {"type": "t", "text": " overload in a Parkin-MCUb-dependent manner."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Metabolism (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.metabol.2023.155551"}], "href": "https://doi.org/10.1016/j.metabol.2023.155551"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36948287"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36948287"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Zhiyuan An, Wenyi Ding "}, {"type": "b", "children": [{"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "Acinetobacter baumannii"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": " up-regulates LncRNA-GAS5 and promotes the degradation of STX17 by blocking the activation of YY1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Virulence (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21505594.2021.1953851"}], "href": "https://doi.org/10.1080/21505594.2021.1953851"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34304694"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34304694"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Xi Wang, Miaoyang Hu, Jingrong Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Key roles of autophagosome/endosome maturation mediated by Syntaxin17 in methamphetamine-induced neuronal damage in mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Med (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s10020-023-00765-9"}], "href": "https://doi.org/10.1186/s10020-023-00765-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38172666"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38172666"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Yueguang Rong, Shen Zhang, Nilay Nandi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "STING controls energy stress-induced autophagy and energy metabolism via STX17."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.202202060"}], "href": "https://doi.org/10.1083/jcb.202202060"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35510944"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35510944"}]}]}]}
Synonyms HSA-MIR-378J
NCBI Gene ID 102465136
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Predicted Functions View MIR378J's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR378J's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR378J's ARCHS4 Predicted Functions.

Functional Associations

MIR378J has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

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Dataset Summary