MIR6722 Gene

HGNC Family Non-coding RNAs
Name microRNA 6722
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 none of the provided abstracts directly mention MIR6722, the collective body of work underscores the central role of calcineurin signaling in diverse physiological and pathological processes. Given that microRNAs are well‐known posttranscriptional regulators, it is reasonable to speculate that MIR6722 may function as a fine tuner of calcineurin pathway components. For example, in T lymphocytes, calcineurin activity is indispensable for activation, cytokine production, and T‐cell survival, as demonstrated by studies showing defective T‐cell development and reduced homeostatic signaling in its absence."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nCalcineurin also plays a critical role in muscle and cardiac biology. In skeletal and cardiac muscle, isoform‐specific actions of calcineurin influence myoblast proliferation, hypertrophic growth, and survival. Studies have documented that an imbalance or loss of specific calcineurin isoforms not only impacts myocardial contractility and apoptosis but also alters metabolic adaptations and fiber‐type identity."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "4", "end_ref": "9"}]}, {"type": "t", "text": " In these tissues, the precision of calcineurin signaling is essential for proper adaptation to stress and injury—a process that MIR6722 might modulate by targeting key mRNAs encoding calcineurin subunits or downstream effectors.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn renal development and disease, calcineurin governs the maturation of nephron structures as well as pathological hypertrophy. Loss of specific calcineurin subunits disrupts nephrogenesis, and altered calcineurin–NFAT signaling is a feature of diabetic renal hypertrophy and other maladaptive responses."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "10", "end_ref": "15"}]}, {"type": "t", "text": " Fine‐tuning of these processes is critical for maintaining renal function under stress, suggesting a potential regulatory role for MIR6722 in modulating calcineurin-driven events.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond muscle and kidney, calcineurin signaling extends to multiple other systems. In insulin-secreting cells, spatially distinct calcineurin activity modulates Ca²⁺ oscillation decoding"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "16"}]}, {"type": "t", "text": ", while in skin, calcineurin–NFAT signaling influences hair follicle development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "17"}]}, {"type": "t", "text": " In metabolic tissues, loss of calcineurin Aβ leads to hyperlipidemia and insulin resistance, implicating aberrant G-protein–coupled receptor signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "18"}]}, {"type": "t", "text": " Moreover, altered calcineurin expression has been linked to changes in endocrine function"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "19"}]}, {"type": "t", "text": ", embryonic stem cell differentiation"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "20"}]}, {"type": "t", "text": ", lung inflammatory responses"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "21"}]}, {"type": "t", "text": ", astrocytic reactivity"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "22"}]}, {"type": "t", "text": ", and responses to mechanical stress in pancreatitis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "23"}]}, {"type": "t", "text": " Vascular remodeling"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "24"}]}, {"type": "t", "text": ", precise neural distribution in the brain"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "25"}]}, {"type": "t", "text": ", and even alterations in tumor energy metabolism"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "26"}]}, {"type": "t", "text": "further exemplify the expansive impact of calcineurin. In these varied contexts, MIR6722 could serve as a key regulatory microRNA, ensuring the spatiotemporal precision of calcineurin-dependent signaling cascades.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn summary, while the current literature does not directly report on MIR6722, the broad and multifaceted roles of calcineurin in immune function, muscle and cardiac biology, renal development, endocrine regulation, and other systems provide a compelling rationale to investigate MIR6722 as a potential modulator of these pathways. Future studies aimed at defining the target mRNAs and regulatory mechanisms of MIR6722 may reveal novel insights into how microRNAs contribute to the fine-tuning of calcineurin-mediated signal transduction and its diverse biological outcomes.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Orlando F Bueno, Eric B Brandt, Marc E Rothenberg, et al. 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Synonyms HSA-MIR-6722
NCBI Gene ID 102465431
API
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Predicted Functions View MIR6722's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR6722's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR6722's ARCHS4 Predicted Functions.

Functional Associations

MIR6722 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

Click the + buttons to view associations for MIR6722 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary