Hily Jean-Michel, Singer Stacy D, Yang Yazhou, Liu Zongrang
USDA-ARS Appalachian Fruit Research Station, 2217 Wiltshire Road, Kearneysville, WV 25430, USA.
Plant Cell Rep. 2009 Jul;28(7):1095-104. doi: 10.1007/s00299-009-0700-8. Epub 2009 Apr 17.
Several matrix-attachment regions (MARs) from animals have been shown to block interactions between an enhancer and promoter when situated between the two. Since a similar function for plant MARs has not been discerned, we tested the Zea mays ADH1 5' MAR, Nicotiana tabacum Rb7 3' MAR and a transformation booster sequence (TBS) MAR from Petunia hybrida for their ability to impede enhancer-promoter interactions in Arabidopsis thaliana. Stable transgenic lines containing vectors in which one of the three MAR elements or a 4 kb control sequence were interposed between the cauliflower mosaic virus 35S enhancer and a flower-specific AGAMOUS second intron-derived promoter (AGIP)::beta-glucuronidase (GUS) fusion were assayed for GUS expression in vegetative tissues. We demonstrate that the TBS MAR element, but not the ADH1 or Rb7 MARs, is able to block interactions between the 35S enhancer and AGIP without compromising the function of either with elements from which they are not insulated.
研究表明,动物的几个基质附着区域(MARs)位于增强子和启动子之间时,会阻断二者之间的相互作用。由于尚未发现植物MARs具有类似功能,我们测试了玉米醇脱氢酶1(Zea mays ADH1)5' MAR、烟草(Nicotiana tabacum)Rb7 3' MAR以及矮牵牛(Petunia hybrida)的转化增强序列(TBS)MAR在拟南芥(Arabidopsis thaliana)中阻断增强子-启动子相互作用的能力。稳定转基因系包含载体,其中三个MAR元件之一或4 kb对照序列插入花椰菜花叶病毒35S增强子与花特异性AGAMOUS第二内含子衍生启动子(AGIP)::β-葡萄糖醛酸酶(GUS)融合体之间,检测这些转基因系营养组织中的GUS表达。我们证明,TBS MAR元件而非ADH1或Rb7 MARs能够阻断35S增强子与AGIP之间的相互作用,同时不影响它们与未隔离元件的功能。