Effects of ADARs on small RNA processing pathways in C. elegans

被引:43
|
作者
Warf, M. Bryan [1 ]
Shepherd, Brent A. [2 ]
Johnson, W. Evan [3 ]
Bass, Brenda L. [1 ]
机构
[1] Univ Utah, Dept Biochem, Salt Lake City, UT 84172 USA
[2] Brigham Young Univ, Dept Stat, Provo, UT 84602 USA
[3] Boston Univ, Dept Med, Boston, MA 02118 USA
关键词
DICERS HELICASE DOMAIN; DOUBLE-STRANDED-RNA; CAENORHABDITIS-ELEGANS; ENDOGENOUS SIRNAS; MESSENGER-RNA; GENE; TRANSCRIPTION; INTERFERENCE; TARGETS; BIOGENESIS;
D O I
10.1101/gr.134841.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adenosine deaminases that act on RNA (ADARs) are RNA editing enzymes that convert adenosine to inosine in double-stranded RNA (dsRNA). To evaluate effects of ADARs on small RNAs that derive from dsRNA precursors, we performed deep-sequencing, comparing small RNAs from wild-type and ADAR mutant Caenorhabditis elegans. While editing in small RNAs was rare, at least 40% of microRNAs had altered levels in at least one ADAR mutant strain, and miRNAs with significantly altered levels had mRNA targets with correspondingly affected levels. About 40% of siRNAs derived from endogenous genes (endo-siRNAs) also had altered levels in at least one mutant strain, including 63% of Dicer-dependent endo-siRNAs. The 26G class of endo-siRNAs was significantly affected by ADARs, and many altered 26G loci had intronic reads and histone modifications associated with transcriptional silencing. Our data indicate that ADARs, through both direct and indirect mechanisms, are important for maintaining wild-type levels of many small RNAs in C. elegans.
引用
收藏
页码:1488 / 1498
页数:11
相关论文
共 50 条
  • [31] Parallel pathways for serotonin biosynthesis and metabolism in C. elegans
    Yu, Jingfang
    Vogt, Merly C.
    Fox, Bennett W.
    Wrobel, Chester J. J.
    Palomino, Diana Fajardo
    Curtis, Brian J.
    Zhang, Bingsen
    Le, Henry H.
    Tauffenberger, Arnaud
    Hobert, Oliver
    Schroeder, Frank C.
    NATURE CHEMICAL BIOLOGY, 2023, 19 (02) : 141 - +
  • [32] Epigenetic Licensing of Germline Gene Expression by Maternal RNA in C. elegans
    Johnson, Cheryl L.
    Spence, Andrew M.
    SCIENCE, 2011, 333 (6047) : 1311 - 1314
  • [33] Parallel Processing of Two Mechanosensory Modalities by a Single Neuron in C. elegans
    Tao, Li
    Porto, Daniel
    Li, Zhaoyu
    Fechner, Sylvia
    Lee, Sol Ah
    Goodman, Miriam B.
    Xu, X. Z. Shawn
    Lu, Hang
    Shen, Kang
    DEVELOPMENTAL CELL, 2019, 51 (05) : 617 - +
  • [34] A fitness assay for comparing RNAi effects across multiple C. elegans genotypes
    Elvin, Mark
    Snoek, Laurens B.
    Frejno, Martin
    Klemstein, Ulrike
    Kammenga, Jan E.
    Poulin, Gino B.
    BMC GENOMICS, 2011, 12
  • [35] On an Analogue Signal Processing Circuit in the Nematode C. elegans
    Skandari, Roghieh
    Iino, Yuichi
    Manton, Jonathan H.
    2016 38TH ANNUAL INTERNATIONAL CONFERENCE OF THE IEEE ENGINEERING IN MEDICINE AND BIOLOGY SOCIETY (EMBC), 2016, : 965 - 968
  • [36] Starvation-Induced Transgenerational Inheritance of Small RNAs in C. elegans
    Rechavi, Oded
    Houri-Ze'evi, Leah
    Anava, Sarit
    Goh, Wee Siong Sho
    Kerk, Sze Yen
    Hannon, Gregory J.
    Hobert, Oliver
    CELL, 2014, 158 (02) : 277 - 287
  • [37] Chromatin Compaction by Small RNAs and the Nuclear RNAi Machinery in C. elegans
    Fields, Brandon D.
    Kennedy, Scott
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [38] An essential role for the piRNA pathway in regulating the ribosomal RNA pool in C. elegans
    Wahba, Lamia
    Hansen, Loren
    Fire, Andrew Z.
    DEVELOPMENTAL CELL, 2021, 56 (16) : 2295 - +
  • [39] Age-related micro-RNA abundance in individual C. elegans
    Lucanic, Mark
    Graham, Jill
    Scott, Gary
    Bhaumik, Dipa
    Benz, Christopher C.
    Hubbard, Alan
    Lithgow, Gordon J.
    Melov, Simon
    AGING-US, 2013, 5 (06): : 394 - 411
  • [40] Caenorhabditis elegans Small RNA Pathways Make Their Mark on Chromatin
    Claycomb, Julie M.
    DNA AND CELL BIOLOGY, 2012, 31 : S17 - S33