RNAi in DNA Sequence Elimination in Tetrahymena

四膜虫 DNA 序列消除中的 RNAi

• 批准号: 7809670
• 负责人: Martin A Gorovsky
• 金额: $ 37.12万
• 依托单位: UNIVERSITY OF ROCHESTER
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-05-01 至 2011-10-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7809670
• 关键词: Affinity Chromatography; Animals; Biology; Boxing; Cell Count; Cell Nucleus; Cell physiology; Cells; Centromere; Chromatin; Cleaved cell; Complex; DNA Sequence; DNA Sequence Rearrangement; DNA Transposable Elements; Development; Double-Stranded RNA; Eukaryota; Genes; Genome; Genome Stability; Germline Micronucleus; Goals; Heterochromatin; Histone H3; Invaded; Light; Lysine; Macronucleus; Maintenance; Mammals; Mediating; Methods; Methylation; Methyltransferase; Molecular; Organism; Play; Process; Property; Protein Family; Proteins; RNA Interference; RNA Viruses; RNA-Directed RNA Polymerase; Regulation; Ribonuclease III; Role; Small Interfering RNA; Small RNA; Staging; System; Testing; Tetrahymena; Tetrahymena thermophila; Transcript; gene replacement; genome sequencing; helicase; human DICER1 protein; insight; interstitial; plant fungi; protein function

DESCRIPTION (provided by applicant): Cells of animals, plants, fungi and protists respond to the presence of intracellular double stranded RNA (dsRNA) by a conserved mechanism (the RNAi machinery), which cleaves dsRNA to small interfering RNAs (siRNAs). While this mechanism likely originated as a defense against invading RNA viruses and transposable elements, similar machineries are used in a variety of important cellular processes to produce specific intracellular RNAs involved in degradation of aberrant transcripts, developmental regulation of utilization of specific mRNAs, heterochromatic silencing, centromere function and maintenance of genome stability by suppression of activity of transposable elements. Genome rearrangement in Tetrahymena involves elimination of about 15% of the genome by reproducible interstitial deletions that occur during development of the somatic macronucleus from the germline micronucleus. This process is controlled by small RNAs that target the sequences for elimination using an RNAi-related mechanism that resembles heterochromatin formation in other eukaryotes. The properties of these small RNAs explain how specific sequences are targeted for elimination and how the primary sequence of the parental macronucleus epigenetically controls genome rearrangement in the new macronucleus. This system provides the first demonstration of an RNAi-mediated process that directly alters DNA sequence organization. Methylation of histone H3 on lysine 9 and accumulation of chromodomain proteins, hallmarks of heterochromatin, also occur specifically on sequences undergoing elimination and are dependent on the small RNAs. These observations contributed to a new paradigm of chromatin biology: targeting of heterochromatin formation by RNAi-related mechanisms in eukaryotes. The elimination process occurs sequentially and can be highly synchronized in a large number of cells. Utilizing recently developed methods for facile gene replacement in either or both the somatic and/or germline nucleus, protein tagging, tandem affinitiy purification and the nearly complete Tetrahymena macronuclear genome sequence, we propose to characterize the molecular mechanism of small RNA-mediated genome reorganization. These studies should shed light on other RNAi- like processes that are important for normal development and maintenance of genome stability in multicellular organisms.

描述（由申请人提供）：动物、植物、真菌和原生生物的细胞通过一种保守机制（RNAi机制）对细胞内双链RNA （dsRNA）的存在做出反应，该机制将dsRNA切割成小干扰RNA （sirna）。虽然这种机制可能起源于防御入侵的RNA病毒和转座元件，但类似的机制在多种重要的细胞过程中被使用，以产生特异性的细胞内RNA，这些RNA参与异常转录物的降解，特定mrna利用的发育调节，异染色质沉默，着丝粒功能和通过抑制转座元件的活性来维持基因组稳定性。在四膜虫中，基因组重排涉及通过可复制的间质缺失消除约15%的基因组，这种缺失发生在体细胞巨核从种系微核发育过程中。这一过程是由小rna控制的，这些小rna利用类似于其他真核生物中异染色质形成的rna相关机制，靶向消除序列。这些小rna的特性解释了特定序列如何被靶向消除，以及亲本大核的初级序列如何在表观遗传学上控制新大核中的基因组重排。该系统首次展示了rnai介导的直接改变DNA序列组织的过程。赖氨酸9上的组蛋白H3甲基化和异染色质的特征——色域蛋白的积累，也特别发生在正在消除的序列上，并且依赖于小rna。这些观察结果促成了染色质生物学的新范式：真核生物中rnai相关机制靶向异染色质形成。消除过程依次发生，并且可以在大量细胞中高度同步。利用最近发展起来的体细胞和/或种系核中的基因替换、蛋白质标记、串联亲和纯化和几乎完整的四膜虫大核基因组序列的方法，我们提出表征小rna介导的基因组重组的分子机制。这些研究将揭示其他类似RNAi的过程，这些过程对多细胞生物的正常发育和基因组稳定性的维持很重要。

项目成果

The nonhistone, N-terminal tail of an essential, chimeric H2A variant regulates mitotic H3-S10 dephosphorylation.

• DOI: 10.1101/gad.182683.111
• 发表时间: 2012-03
• 期刊: Genes & development
• 影响因子: 10.5
• 作者: Xiaoyuan Song;J. Bowen;W. Miao;Yifan Liu;M. Gorovsky

Genome-wide identification and characterization of cytochrome P450 monooxygenase genes in the ciliate Tetrahymena thermophila.

纤毛虫嗜热四膜虫细胞色素 P450 单加氧酶基因的全基因组鉴定和表征

• DOI: 10.1186/1471-2164-10-208
• 发表时间: 2009-05-01
• 期刊: BMC genomics
• 影响因子: 4.4
• 作者: Fu C;Xiong J;Miao W
• 通讯作者: Miao W

Genome-wide identification and evolution of ATP-binding cassette transporters in the ciliate Tetrahymena thermophila: A case of functional divergence in a multigene family.

纤毛虫嗜热四膜虫 ATP 结合盒转运蛋白的全基因组鉴定和进化：多基因家族功能分歧的一个案例

• DOI: 10.1186/1471-2148-10-330
• 发表时间: 2010-10-27
• 期刊: BMC evolutionary biology
• 影响因子: 3.4
• 作者: Xiong J;Feng L;Yuan D;Fu C;Miao W
• 通讯作者: Miao W

The Tetrahymena argonaute-binding protein Giw1p directs a mature argonaute-siRNA complex to the nucleus.

• DOI: 10.1016/j.cell.2010.02.010
• 发表时间: 2010-03-05
• 期刊: Cell
• 影响因子: 64.5
• 作者: Noto T;Kurth HM;Kataoka K;Aronica L;DeSouza LV;Siu KW;Pearlman RE;Gorovsky MA;Mochizuki K
• 通讯作者: Mochizuki K