4.7 Article

Reliability analysis of the Ahringer Caenorhabditis elegans RNAi feeding library: a guide for genomewide screens

Journal

BMC GENOMICS
Volume 12, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/1471-2164-12-170

Keywords

-

Funding

  1. 973 program [2006CB504100]
  2. Natural Science Foundation of China [30900862, 30800196, 30771230]
  3. State Key Laboratory of Proteomics [SKLP-Y200906, SKLP-K201004, SKLP-O201002]
  4. Special Key Programs for Science and Technology of China [2009ZX09503-002, 2009ZX09301-002, 2009ZX09103-616]
  5. Chinese Postdoctoral Science Foundation [200801495, 20060400051]
  6. Beijing Municipal Bureau [7061004]

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Background: The Ahringer C. elegans RNAi feeding library prepared by cloning genomic DNA fragments has been widely used in genome-wide analysis of gene function. However, the library has not been thoroughly validated by direct sequencing, and there are potential errors, including: 1) mis-annotation (the clone with the retired gene name should be remapped to the actual target gene); 2) nonspecific PCR amplification; 3) cross-RNAi; 4) misoperation such as sample loading error, etc. Results: Here we performed a reliability analysis on the Ahringer C. elegans RNAi feeding library, which contains 16,256 bacterial strains, using a bioinformatics approach. Results demonstrated that most (98.3%) of the bacterial strains in the library are reliable. However, we also found that 2,851 (17.54%) bacterial strains need to be reannotated even they are reliable. Most of these bacterial strains are the clones having the retired gene names. Besides, 28 strains are grouped into unreliable category and 226 strains are marginal because of probably expressing unrelated double-stranded RNAs (dsRNAs). The accuracy of the prediction was further confirmed by direct sequencing analysis of 496 bacterial strains. Finally, a freely accessible database named CelRNAi (http://biocompute.bmi.ac.cn/CelRNAi/) was developed as a valuable complement resource for the feeding RNAi library by providing the predicted information on all bacterial strains. Moreover, submission of the direct sequencing result or any other annotations for the bacterial strains to the database are allowed and will be integrated into the CelRNAi database to improve the accuracy of the library. In addition, we provide five candidate primer sets for each of the unreliable and marginal bacterial strains for users to construct an alternative vector for their own RNAi studies. Conclusions: Because of the potential unreliability of the Ahringer C. elegans RNAi feeding library, we strongly suggest the user examine the reliability information of the bacterial strains in the CelRNAi database before performing RNAi experiments, as well as the post-RNAi experiment analysis.

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