Are sperm-borne small RNAs important?
Are sperm-borne small RNAs important?
批准号:
8401509
负责人:
Wei Yan
金额:
$24.65万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-08-01 至 2014-07-31
关键词:
AblationBiogenesisChromatinCongenital AbnormalityCytoplasmDNADataDefectDevelopmentDicer EnzymeEmbryo DeathsEmbryonic DevelopmentEventFailureFertilizationFertilization failureFunctional RNAFunding MechanismsGene Expression ProfileGerm CellsHistonesHumanIn VitroInfertilityInjection of therapeutic agentIntracytoplasmic Sperm InjectionsIonsKaryotypeKnock-outKnockout MiceLeadLifeMessenger RNAMusNegative FindingOocytesPhenotypePhilosophyPhysiologicalPlayPopulationPre-implantation Embryo DevelopmentPromoter RegionsRNAReportingRibonuclease IIIRibonucleasesRoleSiteSmall RNASperm HeadSpermatogenesisSpontaneous abortionTechnologyTestingTimeTranscriptbasecDNA Librarydosageegghigh rewardhigh riskhuman DICER1 proteinmalenext generationnovelpreimplantationpupresearch studysperm cell
中文摘要
描述(由申请人提供):众所周知,小鼠和人类精子在受精过程中携带大量信使RNA和小的非编码RNA进入卵子。 这些父本RNA对受精和早期胚胎发育至关重要吗? 如果是这样的话,这些精子携带的RNA分子一旦进入卵子的细胞质后会做什么? 这些基本问题仍然没有答案,因为这些RNA分子隐藏在高度致密的精子染色质深处。 因此,这些精子携带的RNA种类在不破坏父本DNA的情况下几乎完全不可接近。 我们已经产生了两个条件性敲除小鼠品系,其产生缺乏miRNA和/或内切siRNA的精子。 我们将使用这些小的非编码RNA缺陷的精子进行卵胞浆内单精子注射(ICSI),以观察受精率和早期胚胎发育(Aim 2)。 这些小RNA缺陷精子中的RNA含量也将与正常野生型精子(Aim 1)中的RNA含量进行比较。 阴性结果表明,至少这两种精子携带的小的非编码RNA种类是受精和/或早期胚胎发育的载体。 然而,如果发现这两种小RNA种类对受精和/或胚胎发育至关重要,那么更彻底的研究是
这是有道理的,因为父亲对受精甚至早期胚胎发育的贡献已经假设了很长时间,它代表了关于生命开始所需因素的最基本问题之一。 因此,这项探索性研究符合R2资助机制的高风险、高回报理念。
公共卫生相关性:这项研究将测试两种精子携带的小RNA种类是否是受精和早期胚胎发育所必需的。 这项研究的数据可能会导致发现不孕症,自然流产和出生缺陷的新因素。
英文摘要
DESCRIPTION (provided by applicant): It is well known that both mouse and human sperm carry numerous messenger RNAs and small non-coding RNAs into eggs during fertilization. Are these paternal RNAs essential for fertilization and early embryonic development? If so, what do these sperm-borne RNA molecules do once inside the cytoplasm of the egg? Theses fundamental questions remain unanswered because these RNA molecules are hidden deeply inside the highly compacted sperm chromatin. Thus, these sperm- borne RNA species are almost totally inaccessible without disrupting paternal DNA. We have generated two conditional knockout mouse lines, which produce sperm lacking miRNAs and/or endo-siRNAs. We will use these small non-coding RNA- deficient sperm to perform intracytoplasmic sperm injection (ICSI) to observe the fertilization rate and early embryonic development (Aim2). The RNA contents in these small RNA-deficient sperm will also be defined in comparison to those in normal wild-type sperm (Aim1). A negative finding would suggest that at least these two sperm-borne small non-coding RNA species are dispensable for fertilization and/or early embryonic development. However, if these two small RNA species are found to be essential for fertilization and/or embryonic development, then a more thorough study is
warranted because the paternal contribution to fertilization or even early embryonic development has been hypothesized for a long time and it represents one of the most fundamental questions about factors that are required for the beginning of a life. Therefore, this exploratory study fits the high risk, high reward philosophy of the R2 funding mechanism.
PUBLIC HEALTH RELEVANCE: The study will test whether two of the sperm-;borne small RNA species are required for fertilization and early embryonic development. Data from this study will potentially lead to discoveries of novel factors that are responsble for infertility, spontaneous abortion and birth defects.
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会议论文
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