摘要
用单个植入前胚胎mRNA差别显示方法 (SinglePreimplantationEmbryonicmRNADifferentialDisplayReversePolymeraseReaction ,SPEDDRT PCR) ,以家兔移核重构发育至 2细胞、8细胞时期的胚胎及囊胚作为起始材料。研究家兔移核重构胚再程序化相关基因的表达。获得了 2 5个与再程序化相关的基因片段 ,完成了对所有片段的克隆、序列分析 ,其中 5个反向Northern证实的片段在从MⅡ到囊胚的发育阶段中呈现特异性表达的特点。这项研究为再程序化相关基因全长的分离以及功能研究奠定了良好的基础。
By the method of single preimplantation embryos differential display polymerase chain reaction (SPEDDRT PCR),25 reprogramming cDNA fragments were obtained from single 2 cell,8 cell embryos and blastula. After cloning and sequencing, five of them were identified by reverse Northern and characterized with stage specific expression during reconstructed embryo development. This results will help to isolate full length reprogramming genes and study their function during embryonic development.
出处
《生物工程学报》
CAS
CSCD
北大核心
2003年第1期30-34,共5页
Chinese Journal of Biotechnology
基金
国家重大基础研究发展规划 (973 )资助 (No .2 0 0 0 0 1610 7)~~
关键词
兔移核重构胚
再程序化
相关基因片段
分离
鉴定
cloning, preimplantation embryos, single embryos mRNA differential display, reprogramming