Vernet M, Cebrian J
Institut Cochin de Génétique Molécularire, Laboratoire de Génétique et Pathologie Expérimentales, Unité 380 de l'Institut National de la Santé et de la Recherche Médicale, Paris, France.
J Virol. 1996 Aug;70(8):5630-3. doi: 10.1128/JVI.70.8.5630-5633.1996.
We have addressed the question of the nature of Moloney murine leukemia virus (MoMuLV) repression in mouse embryos by assaying for the transient expression of MoMuLV-derived constructs microinjected into early cleavage embryos. We show that the same cis-acting DNA sequences responsible for the block in MoMuLV expression in embryonal carcinoma cell lines operate in early embryos: (i) the MoMuLV long terminal repeat is nonfunctional, and (ii) the +147 to +163 repressor binding site, or negative regulatory element, negatively regulates the expression from an active promoter.
我们通过检测显微注射到早期卵裂胚胎中的莫洛尼鼠白血病病毒(MoMuLV)衍生构建体的瞬时表达,探讨了小鼠胚胎中MoMuLV抑制的本质问题。我们发现,在胚胎癌细胞系中负责阻断MoMuLV表达的相同顺式作用DNA序列在早期胚胎中也起作用:(i)MoMuLV长末端重复序列无功能,以及(ii)+147至+163阻遏物结合位点或负调控元件对来自活性启动子的表达起负调控作用。