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Yuguo Yuan

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Supervisor of Doctorate Candidates

Master Tutor

Name (English):Yuguo Yuan

Name (Pinyin):Yuan Yuguo

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School/Department:Yangzhou University

Education Level:With Certificate of Graduation for Doctorate Study

Business Address:Wenhui Com[us, 45#,102

Gender:Male

Contact Information:86-514-87979228

Degree:博士

Professional Title:副高级

Status:在岗

Alma Mater:Yangzhou University

Discipline:
Clinical Veterinary Medicine

Honors and Titles:
2024-04-10 elected:动医2002班--江苏省优秀先进班集体(任班主任)
2012-12-14 elected:中国商业联合会科技进步三等奖
2013-01-11 elected:扬州市科技进步二等奖
2013-10-07 elected:动医1002班--江苏省优秀先进班集体(任班主任)
2011-04-12 elected:扬州大学优秀博士论文

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Generation of human lactoferrin transgenic cloned goats using donor cells with dual markers and a modified selection procedure

Date:2022-03-23 clicks:

Impact Factor:2.8

Journal:Theriogenology

Abstract:The objective was to use dual markers to accurately select genetically modified donor cells and ensure that the resulting somatic cell nuclear transfer kids born were transgenic. Fetal fibroblast cells were transfected with dual marking gene vector (pCNLF-ng) that contained the red-shifted variant of the jellyfish green fluorescent protein (LGFP) and neomycin resistance (Neo) markers. Cell clones that were G418-resistant and polymerase chain reaction-positive were subcultured for several passages; individual cells of the clones were examined with fluorescence microscopy to confirm transgenic integration. Clones in which every cell had bright green fluorescence were used as donor cells for nuclear transfer. In total, 86.7% (26/30) cell clones were confirmed to have transgenic integration of the markers by polymerase chain reaction, 76.7% (23/30) exhibited fluorescence, but only 40% (12/30) of these fluorescent cell clones had fluorescence in all cell populations. Moreover, through several cell passages, only 20% (6/30) of the cell clones exhibited stable LGFP expression. Seven transgenic cloned offspring were produced from these cells by nuclear transfer. Overall, the reconstructed embryo fusion rate was 76.6%, pregnancy rates at 35 and 60 days were 39.1% and 21.7%, respectively, and the offspring birth rate was 1.4%. There were no significant differences between nuclear transfer with dual versus a single (Neo) marker (overall, 73.8% embryo fusion rate, 53.8% and 26.9% pregnancy rates, and 1.9% birth rate with five offspring). In conclusion, the use of LGFP/Neo dual markers and an optimized selection procedure reliably screened genetically modified donor cells, excluded pseudotransgenic cells, and led to production of human lactoferrin transgenic goats. Furthermore, the LGFP/Neo markers had no adverse effects on the efficiency of somatic cell nuclear transfer.

Co-author:Yu-Guo Yuan,Yang TJ,Yu BL

First Author:Li-You An

Indexed by:Research Atricle

Correspondence Author:Cheng Y

Translation or Not:no

Date of Publication:2012-10-04

Links to published journals:https://pubmed.ncbi.nlm.nih.gov/22898014/

Pre One:人工锌指核酸酶突变 EGFP 基因的功能分析 Next One:Hybrid expression cassettes consisting of a milk protein promoter and a cytomegalovirus enhancer significantly increase mammary-specific expression of human lactoferrin in transgenic mice