Roux C, Bilang J, Theunissen B H, Perrot-Rechenmann C
Institut des Sciences Végétales, CNRS, Gif sur Yvette, France.
Plant Mol Biol. 1998 May;37(2):385-9. doi: 10.1023/a:1005906316880.
Differential display of mRNA has been improved by developing a two-step PCR amplification procedure. The modified differential display has been applied to identify early alterations of mRNA expression in response to auxin treatment of tobacco seedlings. This approach has led to the isolation of four fragments corresponding to auxin-up-regulated mRNAs. One, named GO15-13, shows significant homology with the 3' end of the coding region of the soybean SAUR X10A. The three other fragments present no homology with sequences available in the databases and constitute potential new early auxin markers.
通过开发两步PCR扩增程序,mRNA差异显示技术得到了改进。改进后的差异显示技术已应用于鉴定烟草幼苗生长素处理后mRNA表达的早期变化。这种方法已导致分离出四个与生长素上调的mRNA相对应的片段。其中一个名为GO15-13的片段与大豆SAUR X10A编码区的3'端具有显著同源性。其他三个片段与数据库中可用的序列没有同源性,构成了潜在的新的早期生长素标记。