Matsumoto T, Wu J, Baba T, Katayose Y, Yamamoto K, Sakata K, Yano M, Sasaki T
Rice Genome Research Program, National Institute of Agrobiological Resources, 2-1-2 Kannondai, Tsukuba, Ibaraki 305-8602, Japan.
Novartis Found Symp. 2001;236:28-38; discussion 38-41. doi: 10.1002/9780470515778.ch4.
Since its establishment in 1991, the Rice Genome Research Program (RGP) has produced some basic tools for rice genome analysis, including a cDNA catalogue, a genetic linkage map and a yeast artificial chromosome (YAC)-based physical map. For the further development of rice genomics, RGP launched in 1998 an international collaborative project on rice genome sequencing. A P1-derived artificial chromosome (PAC)-based, sequence-ready physical map has been constructed using the PCR markers from cDNA sequences (expressed sequence tag [EST] markers). Selected PAC clones with 100-150 kb inserts from chromosomes 1 and 6 have been subjected to shotgun sequencing. The assembled genomic sequences, after predicting the gene-coding region, have been published both through a public database and through our website. As of January 2000, 1.9 Mb from 13 PAC clones were published. Future prospects for understanding rice genomic information at the nucleotide level are discussed.
自1991年成立以来,水稻基因组研究计划(RGP)已开发出一些用于水稻基因组分析的基础工具,包括一个cDNA目录、一张遗传连锁图谱和一张基于酵母人工染色体(YAC)的物理图谱。为了水稻基因组学的进一步发展,RGP于1998年启动了一个水稻基因组测序的国际合作项目。利用来自cDNA序列的PCR标记(表达序列标签[EST]标记)构建了一个基于P1衍生人工染色体(PAC)的、可用于测序的物理图谱。从第1和第6号染色体中挑选出插入片段为100 - 150 kb的PAC克隆进行鸟枪法测序。在预测基因编码区后,组装好的基因组序列已通过公共数据库和我们的网站发布。截至2000年1月,已发布了来自13个PAC克隆的1.9 Mb序列。文中还讨论了在核苷酸水平上理解水稻基因组信息的未来前景。