Literature DB >> 35849200

Increased rates of gene-editing events using a simplified RNAi configuration designed to reduce gene silencing.

Manoj Kumar1, Pankaj Kumar Tripathi1, Dana Ayzenshtat1, Adar Marko1, Zohar Forotan1, Samuel E Bocobza2.   

Abstract

KEY MESSAGE: An optimal RNAi configuration that could restrict gene expression most efficiently was determined. This approach was also used to target PTGS and yielded higher rates of gene-editing events. Although it was characterized long ago, transgene silencing still strongly impairs transgene overexpression, and thus is a major barrier to plant crop gene-editing. The development of strategies that could prevent transgene silencing is therefore essential to the success of gene editing assays. Transgene silencing occurs via the RNA silencing process, which regulates the expression of essential genes and protects the plant from viral infections. The RNA silencing machinery thereby controls central biological processes such as growth, development, genome integrity, and stress resistance. RNA silencing is typically induced by aberrant RNA, that may lack 5' or 3' processing, or may consist in double-stranded or hairpin RNA, and involves DICER and ARGONAUTE family proteins. In this study, RNAi inducing constructs were designed in eleven different configurations and were evaluated for their capacity to induce silencing in Nicotiana spp. using transient and stable transformation assays. Using reporter genes, it was found that the overexpression of a hairpin consisting of a forward tandem inverted repeat that started with an ATG and that was not followed downstream by a transcription terminator, could downregulate gene expression most potently. Furthermore, using this method, the downregulation of the NtSGS3 gene caused a significant increase in transgene expression both in transient and stable transformation assays. This SGS3 silencing approach was also employed in gene-editing assays and caused higher rates of gene-editing events. Taken together, these findings suggested the optimal genetic configuration to cause RNA silencing and showed that this strategy may be used to restrict PTGS during gene-editing experiments.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  ARGAUNOTE7; Betalain; Gene editing; Gene silencing; NtSGS3; PDS; PTGS; Plant transformation; RFP; RNAi

Mesh:

Substances:

Year:  2022        PMID: 35849200     DOI: 10.1007/s00299-022-02903-9

Source DB:  PubMed          Journal:  Plant Cell Rep        ISSN: 0721-7714            Impact factor:   4.964


  66 in total

Review 1.  MicroRNAs: genomics, biogenesis, mechanism, and function.

Authors:  David P Bartel
Journal:  Cell       Date:  2004-01-23       Impact factor: 41.582

Review 2.  RNA silencing in plants.

Authors:  David Baulcombe
Journal:  Nature       Date:  2004-09-16       Impact factor: 49.962

3.  Molecular biology. Amplified silencing.

Authors:  David C Baulcombe
Journal:  Science       Date:  2007-01-12       Impact factor: 47.728

Review 4.  RNA as a target and an initiator of post-transcriptional gene silencing in transgenic plants.

Authors:  D C Baulcombe
Journal:  Plant Mol Biol       Date:  1996-10       Impact factor: 4.076

5.  Epigenetic repeat-induced gene silencing (RIGS) in Arabidopsis.

Authors:  F F Assaad; K L Tucker; E R Signer
Journal:  Plant Mol Biol       Date:  1993-09       Impact factor: 4.076

6.  Specific and heritable genetic interference by double-stranded RNA in Arabidopsis thaliana.

Authors:  C F Chuang; E M Meyerowitz
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

7.  Stable high-level transgene expression in Arabidopsis thaliana using gene silencing mutants and matrix attachment regions.

Authors:  Katleen M J Butaye; Inge J W M Goderis; Piet F J Wouters; Jonathan M-T G Pues; Stijn L Delauré; Willem F Broekaert; Ann Depicker; Bruno P A Cammue; Miguel F C De Bolle
Journal:  Plant J       Date:  2004-08       Impact factor: 6.417

8.  Nuclear gene silencing directs reception of long-distance mRNA silencing in Arabidopsis.

Authors:  C A Brosnan; N Mitter; M Christie; N A Smith; P M Waterhouse; B J Carroll
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-04       Impact factor: 11.205

Review 9.  A Fruitful Decade Using Synthetic Promoters in the Improvement of Transgenic Plants.

Authors:  Sajid Ali; Won-Chan Kim
Journal:  Front Plant Sci       Date:  2019-11-01       Impact factor: 5.753

10.  Simultaneous knockdown of six non-family genes using a single synthetic RNAi fragment in Arabidopsis thaliana.

Authors:  Olaf Czarnecki; Anthony C Bryan; Sara S Jawdy; Xiaohan Yang; Zong-Ming Cheng; Jin-Gui Chen; Gerald A Tuskan
Journal:  Plant Methods       Date:  2016-02-17       Impact factor: 4.993

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