MIR6738 Gene

HGNC Family Non-coding RNAs
Name microRNA 6738
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 initial query referenced MIR6738, none of the provided abstracts mention or characterize MIR6738. Instead, these studies collectively detail the critical functions of the LIM‐homeobox transcription factors Lhx1 and Lhx5 in neuronal development. In the developing spinal cord, Lhx1 and Lhx5 are required in multiple inhibitory interneuron lineages to sustain the expression of Pax genes, particularly Pax2, which is essential for establishing and maintaining a GABAergic identity in dorsal interneurons."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n\nIn the cerebellum, Lhx1 and Lhx5 are indispensable for Purkinje cell differentiation. One study showed that loss of these factors in early Purkinje cell precursors leads to a marked reduction of Purkinje cells"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": ", whereas a separate investigation demonstrated that in postnatal Purkinje cells Lhx1/5 regulate dendritic development and spine morphogenesis by transcriptionally activating Espin, an F‐actin regulator. This regulation ensures proper synapse formation and functional integration within cerebellar circuits."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n\nIn the developing forebrain, particularly within the telencephalon, Lhx1 and Lhx5 orchestrate the generation and correct distribution of Cajal–Retzius cells by modulating reelin expression and cell migration patterns. Disruption of Lhx5 leads to a reduced number of reelin-positive cells and the emergence of ectopic clusters, underscoring its complex role in cortical lamination."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n\nAdditionally, analysis of various LIM‐homeodomain factors in the inner ear reveals that Lhx5 is expressed in differentiating sensory epithelia and in ganglion neurons. Its overlapping expression with other LIM factors suggests a redundant yet significant role in the patterning and differentiation of inner ear cell types."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Andrea Pillai, Ahmed Mansouri, Richard Behringer, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Lhx1 and Lhx5 maintain the inhibitory-neurotransmitter status of interneurons in the dorsal spinal cord."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Development (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/dev.02717"}], "href": "https://doi.org/10.1242/dev.02717"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17166926"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17166926"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Yangu Zhao, Kin-Ming Kwan, Christina M Mailloux, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LIM-homeodomain proteins Lhx1 and Lhx5, and their cofactor Ldb1, control Purkinje cell differentiation in the developing cerebellum."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.0705464104"}], "href": "https://doi.org/10.1073/pnas.0705464104"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17664423"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17664423"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Nga Chu Lui, Wing Yip Tam, Caiji Gao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Lhx1/5 control dendritogenesis and spine morphogenesis of Purkinje cells via regulation of Espin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncomms15079"}], "href": "https://doi.org/10.1038/ncomms15079"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28516904"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28516904"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Amaya Miquelajáuregui, Alfredo Varela-Echavarría, M Laura Ceci, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LIM-homeobox gene Lhx5 is required for normal development of Cajal-Retzius cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1523/JNEUROSCI.5563-09.2010"}], "href": "https://doi.org/10.1523/JNEUROSCI.5563-09.2010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20685998"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20685998"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Mingqian Huang, Cyrille Sage, Huawei Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Diverse expression patterns of LIM-homeodomain transcription factors (LIM-HDs) in mammalian inner ear development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Dev Dyn (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/dvdy.21735"}], "href": "https://doi.org/10.1002/dvdy.21735"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18942141"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18942141"}]}]}]}
Synonyms HSA-MIR-6738
NCBI Gene ID 102465442
API
Download Associations
Predicted Functions View MIR6738's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR6738's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR6738's ARCHS4 Predicted Functions.

Functional Associations

MIR6738 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

Click the + buttons to view associations for MIR6738 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary