Kosman Dave, Mizutani Claudia M, Lemons Derek, Cox W Gregory, McGinnis William, Bier Ethan
Section of Cell and Developmental Biology, University of California-San Diego, La Jolla, CA 92093, USA.
Science. 2004 Aug 6;305(5685):846. doi: 10.1126/science.1099247.
We present a fluorescence-based, multiplex in situ hybridization method that permits the simultaneous detection of five differently labeled antisense RNA probes and up to seven differ-ent transcripts in a single Drosophila embryo. We also show that it should be possible to increase the number of detected transcripts substantially with nascent transcript multiplex fluorescent in situ hybridization. These multiplex methods fill a current technological gap between high-resolution in situ hybridization with one or two fluorescently labeled probes and low-resolution but genome-wide microarray RNA profiling and should be of great utility in establishing gene networks.
我们展示了一种基于荧光的多重原位杂交方法,该方法能够在单个果蝇胚胎中同时检测五个不同标记的反义RNA探针以及多达七种不同的转录本。我们还表明,通过新生转录本多重荧光原位杂交,大幅增加检测到的转录本数量应该是可行的。这些多重方法填补了当前在使用一两个荧光标记探针进行高分辨率原位杂交与低分辨率但全基因组微阵列RNA分析之间的技术空白,并且在建立基因网络方面应该具有很大的实用性。