Creating a novel method for chicken primordial germ cell health monitoring using the fluorescent ubiquitination-based cell cycle indicator reporter system

被引:0
|
作者
Ecker, Andras [1 ]
Lazar, Bence [1 ,2 ]
Toth, Roland I. [1 ]
Urban, Martin [1 ]
Hoffmann, Orsolya I. [1 ,2 ]
Fekete, Zsofia [1 ,4 ]
Barta, Endre [1 ,5 ]
Uher, Ferenc [6 ]
Matula, Zsolt [6 ]
Varkonyi, Eszter [3 ]
Gocza, Elen [1 ,2 ]
机构
[1] Hungarian Univ Agr & Life Sci, Inst Genet & Biotechnol, H-2100 Godollo, Hungary
[2] Agribiotechnol & Prec Breeding Food Secur Natl Lab, H-2100 Godollo, Hungary
[3] Natl Ctr Biodivers & Gene Conservat, H-2100 Godollo, Hungary
[4] Univ Eastern Finland, Dept Environm & Biol Sci, Joensuu 80101, Finland
[5] Univ Debrecen, Fac Med, Dept Biochem & Mol Biol, H-4032 Debrecen, Hungary
[6] Natl Inst Hematol & Infectol, H-1097 Budapest, Hungary
关键词
chicken; PGC; FUCCI; transgenesis; cell cycle monitoring; EMBRYONIC STEM-CELLS; CANCER-CELLS; IN-VITRO; FUCCI; REPLICATION; MIGRATION; DYNAMICS; PHASE; GENE; CRYOPRESERVATION;
D O I
10.1016/j.psj.2024.104144
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The most current in vitro genetic methods, including gene preservation, gene editing and developmental modelling, require a significant number of healthy cells. In poultry species, primordial germ cells (PGCs) are great candidates for all the above-mentioned purposes, given their easy culturing and well-established freezing method for chicken. However, the constant monitoring of cultures can be financially challenging and consumes large amounts of solutions and accessories. This study aimed to introduce the Fluorescent Ubiquitinationbased Cell Cycle Indicator (FUCCI) complex into the chicken PGCs. FUCCI is a powerful transgenic tool based on the periodic protein expression changes during the cell cycle. It includes chromatin licensing and DNA replication factor 1 attached monomeric Kusabira-Orange and Geminin-attached monomeric Azami-Green fluorescent proteins, that cause the cells to express a red signal in the G1 phase and a green signal in S and G2 phases. Modification of the chicken PGCs was done via electroporation and deemed to be successful according to confocal microscopy, DNA sequencing and timelapse video analysis. Stable clone cell lines were established, cryopreserved, and injected into recipient embryos to prove the integrational competency. The cell health monitoring was tested with medium change experiments, that proved the intended reactions of the FUCCI transgene. These results established the future for FUCCI experiments in chicken, including heat treatment and toxin treatment.
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页数:12
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