| HGNC Family | Non-coding RNAs |
| Name | microRNA 521-2 |
| 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 studies provided focus on the critical role of the manchette protein IQ motif‐containing N (IQCN) in male fertility. In one investigation, the authors posed the question of how defects in IQCN affect sperm flagellar assembly, suggesting that IQCN is integral to the proper formation of specialized sperm structures needed for correct flagellar organization and subsequent function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nA complementary study identified a homozygous frameshift variant in IQCN in a man suffering from unexplained infertility. Here, reduced levels of IQCN mRNA and undetectable protein were associated with abnormal sperm morphology and function, culminating in fertilization failure. The study was corroborated by an Iqcn knockout mouse model, underscoring the gene’s importance in sperm motility and fertilization, and establishing its autosomal-recessive mode of action in male infertility."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAlthough the question initially asked for a summary of the function of MIR521-2, no direct information regarding MIR521-2 is provided in these abstracts. Instead, the reported findings delineate the essential function of IQCN in sperm structural integrity and fertilization. Future studies may explore whether microRNAs such as MIR521-2 play regulatory roles in IQCN expression or spermatogenesis, but based on the current data, the function of MIR521-2 remains to be elucidated.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Qi Li, Yize Wang, Wei Zheng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Reprod (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/humrep/dead079"}], "href": "https://doi.org/10.1093/humrep/dead079"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37140151"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37140151"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Yulin Wang, Guoyong Chen, Zhenzhen Tang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Loss-of-function mutations in IQCN cause male infertility in humans and mice owing to total fertilization failure."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Hum Reprod (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/molehr/gaad018"}], "href": "https://doi.org/10.1093/molehr/gaad018"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37184908"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37184908"}]}]}]}
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| Synonyms | MIR-521-2, MIRN521-2 |
| NCBI Gene ID | 574481 |
| 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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MIR521-2 has 189 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 8 datasets.
Click the + buttons to view associations for MIR521-2 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 MIR521-2 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR521-2 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 MIR521-2 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 MIR521-2 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR521-2 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR521-2 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 MIR521-2 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR521-2 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |