Li Wen, Lu Guang-Xiu
Insitute of Reproductive and Stem Cell Engineering, Central South University, Changsha, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Apr;32(2):252-8.
To investigate the differences of gene expression before and after the compaction to search for the control mechanism of compaction.
8-cell embryos (626 mice) and 8-cell compacted embryos (437 mice) were collected from Kunmingbai mice, respectively. The cDNA of early 8-cell embryos was used as a tester, and the cDNA of 8-cell compacted embryos as a driver. Differences of gene expression were investigated between early 8-cell embryos and 8-cell compacted embryos using combining SMART (switching mechanism at 5o end of the RNA transcript) -PCR and suppression subtractive hybridization (SSH).
Four hundreds and seventy eight positive clones were obtained, of which 384 clones with a range of 200~1000 bp and low redundancy were selected for further analysis. Eighty-three ESTs (expressed sequence tags) of the genes expressed differently were gained between early 8-cell embryos and 8-cell compacted embryos. Bioinformatic analysis showed that among the screened 83 putative positive ESTs, 51 ESTs matched 36 known genes, 27 ESTs matched 7 hypothetical genes, and 5 ESTs were new. Genes, which were up-regulated during the compaction, included cytoskeleton(4.8%); enzymes (9.6%); transcriptional factor/regulatory factor (12%); binding protein, protein-protein interactions and transport(13.3%); structural constituent of ribosome (14.5%); pluripotency associated gene(27.7%), and molecular function unknown(18%). Novel ESTs and 17 ESTs which matched the hypothetical genes were put into GenBank with accession numbers.
Combining SMART-PCR and suppression subtractive hybridization is an efficient method to investigate the gene expression difference in a few samples. During the compaction, the genes maintaining cell pluripotentiality express actively, which may be related to maintaining the embryonic cell totipotence in the differentation environment. All the 17 ESTs might be novel genes related to the compaction in the compacted embryos.
研究致密化前后基因表达的差异,以探寻致密化的调控机制。
分别从昆明小鼠中收集8细胞胚胎(626只小鼠)和8细胞致密化胚胎(437只小鼠)。以早期8细胞胚胎的cDNA作为检测子,8细胞致密化胚胎的cDNA作为驱动子。采用SMART(RNA转录本5'端转换机制)-PCR与抑制性消减杂交(SSH)相结合的方法,研究早期8细胞胚胎与8细胞致密化胚胎之间基因表达的差异。
获得478个阳性克隆,从中选取384个长度在200~1000 bp、冗余度低的克隆进行进一步分析。在早期8细胞胚胎与8细胞致密化胚胎之间获得了83个表达差异基因的EST(表达序列标签)。生物信息学分析表明,在筛选出的83个推定阳性EST中,51个EST与36个已知基因匹配,27个EST与7个假定基因匹配,5个EST为新基因。在致密化过程中上调的基因包括细胞骨架(4.8%);酶(9.6%);转录因子/调控因子(12%);结合蛋白、蛋白质-蛋白质相互作用和转运(13.3%);核糖体结构成分(14.5%);多能性相关基因(27.7%),以及分子功能未知(18%)。将新的EST和17个与假定基因匹配的EST提交至GenBank并获得登录号。
SMART-PCR与抑制性消减杂交相结合是研究少量样本中基因表达差异的有效方法。在致密化过程中,维持细胞多能性的基因活跃表达,这可能与在分化环境中维持胚胎细胞全能性有关。所有17个EST可能是致密化胚胎中与致密化相关的新基因。