期刊文献+

兔单个植入前克隆胚胎cDNA文库的构建 被引量:7

Construction of cDNA Library from Rabbit Single Preimplantation Cloned Embryos
下载PDF
导出
摘要 人与小鼠和牛在正常胚胎植入前发育过程中基因活化的研究已经取得了长足的进展 ,但是还没有对同期克隆胚胎相关研究的报道 .利用单个家兔植入前移核重构胚胎成功地构建了MⅡ卵母细胞及发育至 4 、8 细胞期的胚胎和囊胚的特异性cDNA文库 .并用 β肌动蛋白和LAPTM4α证实这类文库是可靠的 .以 8 细胞期移核重构胚cDNA文库为例 ,随机挑取克隆进行测序分析 :其中 2 3的基因EST片段可以在GenBank或EST库中找到同源序列 ,约 1 3的EST片段属于未知的新片段 ,表明这是一类重要的新兴基因资源库 (期特异性EST库 ) .这种利用单胚胎构建cDNA文库的方法 ,解决了胚胎研究材料受限的问题 ,在时间上更加精确 ,更符合胚胎发育的规律 ,也能够更加准确地反映出一些克隆胚胎的异常表型 ,是研究早期胚胎发育基因表达以及克隆胚胎再程序化基因表达的一种有效手段 . The gene activity during rabbit preimplantation cloned embryos development has not been reported,despite great progress having been made recently about normal preimplantation development in human,mouse and bovine.The stage\|specific cDNA libraries were constructed from single four\|cell,eight\|cell and blastocyte embryos,respectively.They have average complexities of 1 0×10\+6 independent clones.From the single eight\|cell cDNA libraries,13 clones were randomly selected to sequence.2/3 of the sequence were homologous to known transcripts or expressed sequence tags (ESTs) from human,mouse,and bovine.Novel sequences were detected at a frequency of 1/3.Reverse Northern blot analyses of specific and general genes (LAPTM4α and β\|actin) proved the credibility of these libraries.These cDNA libraries are a valuable resource for the isolation of clones representing genes and nuclear reprogramming active at these early development stage.
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2004年第2期162-165,共4页 Chinese Journal of Biochemistry and Molecular Biology
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 基因活化 克隆 胚胎 CDNA文库 rabbit preimplantation development,embryonic expression libraries,reprogramming related gene,ESTs,nuclear transfer
  • 相关文献

参考文献17

  • 1De Sousa P A, Caveney A, Westhusin M E, Watson A J. Temporal patterns of embryonic gene expression and their dependence on oogenetic factors. Theriogenology, 1998,49:115 - 128 被引量:1
  • 2Ponsuksili S, Wimmers K, Adjaye J Schellander K. A source for expression profiling in single preimplantation bovine embryos.Theriogenology, 2002,57: 1611 - 1624 被引量:1
  • 3Rideout W M 3rd, Eggan K, Jaenisch. Nuclear cloning and epigenetic reprogramming of genome. Science, 2001.293: 1093 - 1098 被引量:1
  • 4Wilmut I, Schnieke A E, McWhir J. Viable offspring derived from fetal and adult mammalian cells. Nature, 1997,385:810- 813 被引量:1
  • 5Beliavsky A, Vinogradova T Rajewsky K. PCR-based cDNA library construction: general cDNA libraries at the level of a few cells. Nucleic Acids Res, 1989, 17: 2919-2923 被引量:2
  • 6Brady G, Billia F, Knox J . Analysis of gene expression in a complex differentiation hierarchy by global amplification of cDNA from single cell. Curr Biol, 1995, 5:909 - 922 被引量:2
  • 7Dulac C, Axel R. A novel family of genes encoding putative pheromone receptors in mammals. Cell, 1995,83:195 - 206 被引量:1
  • 8Amrein H, Axel R. Gene expressed in neurons of adult male Drosophila. Cell, 1997,88: 459 - 469 被引量:2
  • 9Adjaye J, Daniel R, Bolton V , Monk M. cDNA libaraies from single human preimplantion embryos. Genomics, 1997.46:337 - 344 被引量:1
  • 10Adjaye J, Daniel R,Monk M. The construction of cDNA libraries from human single preimplantation embryos and their use in the study of gene expression during development. J Assist Reprod Genet, 1998,15(5): 344~ 348 被引量:1

二级参考文献20

  • 1Shimono A, Behringer R R. Differential screens with subtracted PCR-generated cDNA libraries from subregions of single mouse embryos. Methods Mol Biol, 2000, 1 (136): 333~344. 被引量:1
  • 2Liang P, Pardee A B. Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. Science, 1992,257 (5072): 967--971. 被引量:1
  • 3Robert C, Barnes F L, Hue I, et al. Subtractive hybridization used to identify mRNA associated with the maturation of bovine oocyte. Mol Reprod Dev, 2000, 57 (2): 167--175. 被引量:1
  • 4Conway G. Novel gene expressed during Zebrafish gastrulation identified by differential RNA display. Mech Dev, 1995, S2 (2--3):. 383--387. 被引量:1
  • 5Li S H, Han W H. mRNA differential display and its applicatition to the identification of development related genes. Dev Rep Biol,1997, 6 (2): 67--75. 被引量:1
  • 6Atale D R, Kidder G M, Westhusin M E, et al. Assessment by differential display-RT-PCR of mRNA transitions and α amanitin sensitivity during bovine perattachment development. Mol Reprod Dev, 2000, 55 (2): 152--163. 被引量:1
  • 7Adjays J, Daniel R, Bolton V, et al. cDNA libaraies from single human preimplantion embryos. Genomics, 1997, 46 (6) : 337--344. 被引量:1
  • 8Henrign G, Renard J P, Chesne P, et al. Diffreential regulation of the translation and the stability of two maternal transcripts in preimplantation rabbit embryos. Mol Reprod Dev, 2000,(1): 12--25. 被引量:1
  • 9Zimmermarm J W, Schultz R M. Analysis of gene expression in the preimplantation mouse embryo: Use of mRNA differential dispay.Dev Biol, 1994, 91 (12): 5456--5460. 被引量:1
  • 10Naojiro M, Kana S, Akira A, et al. Analysis of gene expression in mouse 2-cell embryos using fluorescein differential display:comparison of culture environments. Biol Reprod, 2001, 64 (1) :30--35. 被引量:1

共引文献32

同被引文献115

引证文献7

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部