Using a nano-flare probe to detect RNA in live donor cells prior to somatic cell nuclear transfer

• Published in: Cell biology international 2016-01, Vol.40 (1), p.7-15
• Main Authors: Fu, Bo, Ren, Liang, Liu, Di, Ma, Jian-zhang, An, Tie-zhu, Yang, Xiu-qin, Ma, Hong, Guo, Zhen-hua, Zhu, Meng, Bai, Jing
• Format: Article
• Language: English
• Subjects: Animals; Animals, Genetically Modified; Carbocyanines - chemistry; Cloning; Cloning, Organism; Cytotoxicity; development; Female; Fibroblasts; Fibroblasts - cytology; Fluorescent Dyes - chemistry; Gene Expression; Gene Silencing; Genetic Engineering; In Situ Hybridization, Fluorescence - methods; Metal Nanoparticles; nanoparticle; Nuclear Transfer Techniques; Nucleic Acid Hybridization - methods; Oocytes - cytology; Oocytes - metabolism; RNA detection; RNA, Ribosomal, 18S - analysis; RNA, Ribosomal, 18S - genetics; somatic cell nuclear transfer; Swine; Tissue Donors; Transgenes; Transplants & implants
• ISSN: 1065-6995; 1095-8355
• DOI: 10.1002/cbin.10504

Many transgenes are silenced in mammalian cells (donor cells used for somatic cell nuclear transfer [SCNT]). Silencing correlated with a repressed chromatin structure or suppressed promoter, and it impeded the production of transgenic animals. Gene transcription studies in live cells are challenging because of the drawbacks of reverse‐transcription polymerase chain reaction and fluorescence in situ hybridization. Nano‐flare probes provide an effective approach to detect RNA in living cells. We used 18S RNA, a housekeeping gene, as a reference gene. This study aimed to establish a platform to detect RNA in single living donor cells using a Nano‐flare probe prior to SCNT and to verify the safety and validity of the Nano‐flare probe in order to provide a technical foundation for rescuing silenced transgenes in transgenic cloned embryos. We investigated cytotoxic effect of the 18S RNA–Nano‐flare probe on porcine fetal fibroblasts, characterized the distribution of the 18S RNA–Nano‐flare probe in living cells and investigated the effect of the 18S RNA–Nano‐flare probe on the development of cloned embryos after SCNT. The cytotoxic effect of the 18S RNA–Nano‐flare probe on porcine fetal fibroblasts was dose‐dependent, and 18S RNA was detected using the 18S RNA–Nano‐flare probe. In addition, treating donor cells with 500 pM 18S RNA–Nano‐flare probe did not have adverse effects on the development of SCNT embryos at the pre‐implantation stage. In conclusion, we established a preliminary platform to detect RNA in live donor cells using a Nano‐flare probe prior to SCNT.