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Recent Advances and Future Perspectives of In Vivo Targeted Delivery of Genome-Editing Reagents to Germ cells, Embryos, and Fetuses in Mice
 
 
Article
Peer-Review Record

Modification of i-GONAD Suitable for Production of Genome-Edited C57BL/6 Inbred Mouse Strain

by Yukari Kobayashi 1, Takuya Aoshima 1, Ryota Ito 1, Ryota Shinmura 1, Masato Ohtsuka 2,3,4, Eri Akasaka 5, Masahiro Sato 5,* and Shuji Takabayashi 1,*
Reviewer 1: Anonymous
Reviewer 2:
Submission received: 13 March 2020 / Revised: 7 April 2020 / Accepted: 10 April 2020 / Published: 13 April 2020
(This article belongs to the Special Issue Genome Editing Systems, Methods, Techniques and Their Application)

Round 1

Reviewer 1 Report

The manuscript is well-written. The results are also clear to show that i-GONAD is an efficient technology. Only minor comments from me. I know the authors have used PCR sequencing to check the indels. However, it would further improve the paper if the authors show the % of editing at the locus (efficiency) at the same time in Figure 2, 3 and 4. 

 

 

Author Response

Reviewer 1

Answer: We are thankful for the reviewer’s cordial comments. As suggested by the reviewer, we included data on the genome editing efficiency (%) as Tables in the bottom of each Figure (see Figures 2d, 3d and 4d in the revised text)”. Concomitantly, we added phrases (shown in red) in the legend of each figure in the revised text.

Author Response File: Author Response.docx

Reviewer 2 Report

In this study, Kobayashi and collabs investigated the optimal current (mA) required in iGONAD delivery of RNPs for CRISPR gene editing of mice. A secondary aim of the study was to observe if application of the PMSG hormone to females prior mating increases the pregnancy success rate in C57BL6 mice. Both aims of the study are well described, designed experimentally and presented. I have no further comments for the authors.

Author Response

Reviewer 2

Thank you for revising our manuscript. The comment raised by the referee encourages our on-going study.

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