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Ovarian Kaleidoscope Database (OKdb)

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microRNA 200b OKDB#: 5412
 Symbols: MIR200B Species: human
 Synonyms: MIRN200B, mir-200b  Locus: 1p36.33 in Homo sapiens


For retrieval of Nucleotide and Amino Acid sequences please go to: OMIM Entrez Gene
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General Comment NCBI Summary: 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]
General function RNA metabolism
Comment
Cellular localization
Comment
Ovarian function
Comment
Expression regulated by
Comment
Ovarian localization serum
Comment Elevated circulating micro-ribonucleic acid (miRNA)-200b and miRNA-429 levels in anovulatory women. Eisenberg I et al. (2016) To study the role of micro-RNA (miRNA)-200b and miRNA-429 in human ovulation and to measure their expression levels in ovulatory and anovulatory patients. Micro-RNA-200b and miRNA-429 expression analysis in human serum and granulosa cells at different phases of the ovulation cycle in normal cycling women and women undergoing assisted reproductive technology cycles. University-affiliated hospital and academic research laboratory. Forty women (7 normally ovulating, 15 normally ovulating with pure male infertility factor, and 18 with polycystic ovary syndrome) were included in this study. None. The expression profile of circulating miRNAs and granulosa cells was assessed by means of real-time quantitative reverse transcription-polymerase chain reaction analysis. We identified miRNA-200b and miRNA-429 in the sera of all women tested. These miRNA expression levels were elevated during the early follicular phase of the cycle compared with serum levels during the early luteal phase. Anovulatory women, diagnosed with polycystic ovary syndrome, expressed significantly higher levels of miRNA-200b and miRNA-429 compared with spontaneously ovulating women. Ovulation induction with exogenous gonadotropins during an IVF cycle reduced these levels to the levels measured in normal ovulating women. Our findings suggest an involvement of miRNA-200b and miRNA-429 in the pituitary regulation of human ovulation. Although it is unclear whether this altered miRNA expression profile is a cause or a result of anovulation, the levels of these molecules in the serum of anovulatory women may serve as serum biomarkers for the ovulation process.//////////////////
Follicle stages
Comment
Phenotypes PCO (polycystic ovarian syndrome)
Mutations 1 mutations

Species: None
Mutation name:
type: null mutation
fertility: infertile - ovarian defect
Comment: The miRNA-200 cluster on chromosome 23 is required for oocyte maturation and ovulation in zebrafish. Xiong S et al. (2020) The reproductive process is usually controlled by the hypothalamic-pituitary-gonad (HPG) axis in vertebrates, while Kiss/GnRH system in the hypothalamus is required for mammalian reproduction but dispensable for fish reproduction. The regulation of FSH/LH expression in fish species is still unknown. Here, we identified miR-200 s on chromosome 23 (chr23-miR-200 s) as important regulators for female zebrafish reproduction. Knockout of chr23-miR-200 s (chr23-miR-200 s-KO) resulted in dysregulated expression of lhb and some hormone genes in the pituitary as revealed by comparative transcriptome profiling, leading to failure of oocyte maturation and ovulation as well as defects in reproductive duct development. Chr23-miR-200 s mainly expressed in the pituitary and regulated lhb expression by targeting the transcription repressor wt1a. Injection of hCG could rescue the defects of oocyte maturation in chr23-miR-200 s-KO zebrafish, whereas GnRH or LHRH-A2 could not, suggesting that Chr23-miR-200 s regulated lhb expression in a GnRH-independent pathway. It was remarkable that either injection of carp pituitary extraction (CPE), or co-injection of hCG with synthetic Oxytocin and Vasotocin could greatly rescue the defects of both oocyte maturation and ovulation in chr23-miR-200 s-KO zebrafish. Altogether, our findings highlight an important function of chr23-miR-200 s in controlling oocyte maturation by regulation LH expression, and Oxytocin and Vasotocin are potentially responsible for the ovulation in fish species.//////////////////

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created: Nov. 8, 2016, 10:02 a.m. by: system   email:
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last update: July 29, 2020, 1:43 p.m. by: hsueh    email:



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