RNA interference may result in unexpected phenotypes in Caenorhabditis elegans

被引:17
|
作者
De-Souza, Evandro A. [1 ,2 ]
Camara, Henrique [1 ,3 ,4 ]
Salgueiro, Willian G. [3 ,4 ]
Moro, Raissa P. [3 ,4 ]
Knittel, Thiago L. [3 ,4 ]
Tonon, Guilherme [3 ,4 ]
Pinto, Silas [1 ,3 ,4 ]
Pinca, Ana Paula F. [1 ]
Antebi, Adam [5 ,6 ]
Pasquinelli, Amy E. [7 ]
Massirer, Katlin B. [4 ,8 ,9 ]
Mori, Marcelo A. [1 ,3 ,4 ]
机构
[1] Univ Fed Sao Paulo, Program Mol Biol, BR-04044020 Sao Paulo, Brazil
[2] Univ Fed Rio de Janeiro, Inst Bioquim Med Leopoldo de Meis, Program Mol Biol & Biotechnol, BR-21941902 Rio De Janeiro, Brazil
[3] Univ Estadual Campinas, Dept Biochem & Tissue Biol, BR-13083862 Campinas, SP, Brazil
[4] Univ Estadual Campinas, Program Genet & Mol Biol, BR-13083970 Campinas, SP, Brazil
[5] Max Planck Inst Biol Ageing, D-50931 Cologne, Germany
[6] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany
[7] Univ Calif San Diego, Div Biol, La Jolla, CA 92093 USA
[8] Univ Estadual Campinas, CBMEG UNICAMP, Ctr Mol Biol & Genet Engn, BR-13083875 Campinas, SP, Brazil
[9] Univ Estadual Campinas, Struct Genom Consortium UNICAMP, BR-13083875 Campinas, SP, Brazil
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
DOUBLE-STRANDED-RNA; C-ELEGANS; LIFE-SPAN; GENETIC INTERFERENCE; FUNCTIONAL-ANALYSIS; BODY-SIZE; EXPRESSION; PROTEIN; MECHANISMS; MICRORNAS;
D O I
10.1093/nar/gkz154
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
RNA interference (RNAi) is a valuable technique to determine gene function. In Caenorhabditis elegans, RNAi can be achieved by feeding worms bacteria carrying a plasmid expressing double-stranded RNA (dsRNA) targeting a gene of interest. The most commonly used plasmid vector for this purpose is L4440. However, it has been noticed that sequences within L4440 may elicit unspecific effects. Here, we provide a comprehensive characterization of these effects and their mechanisms and describe new unexpected phenotypes uncovered by the administration of unspecific exogenous dsRNA. An example involves dsRNA produced by the multiple cloning site (MCS) of L4440, which shares complementary sequences with some widely used reporter vectors and induces partial transgene silencing via the canonical and antiviral RNAi pathway. Going beyond transgene silencing, we found that the reduced embryonic viability of mir-35-41(gk262) mutants is partially reversed by exogenous dsRNA via a mechanism that involves canonical RNAi. These results indicate cross-regulation between different small RNA pathways in C. elegans to regulate embryonic viability. Recognition of the possible unspecific effects elicited by RNAi vectors is important for rigorous interpretation of results from RNAi-based experiments.
引用
收藏
页码:3957 / 3969
页数:13
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