Watanabe Junichi, Suzuki Yutaka, Sasaki Masahide, Sugano Sumio
Department of Parasitology, Human Genome Center, Institute of Medical Science, The University of Tokyo, 4-6-1, Shirokanedai, Minatoku, Tokyo 108-8639, Japan.
Nucleic Acids Res. 2004 Jan 1;32(Database issue):D334-8. doi: 10.1093/nar/gkh115.
Full-malaria (http://fullmal.ims.u-tokyo.ac.jp), a database for full-length cDNAs from the human malaria parasite, Plasmodium falciparum has been updated in at least three points. (i) We added 8934 sequences generated from the addition of new libraries, so that our collection of 11,424 full-length cDNAs covers 1375 (25%) of the estimated number of the entire 5409 parasite genes. (ii) All of our full-length cDNAs and GenBank EST sequences were mapped to genomic sequences together with publicly available annotated genes and other predictions. This precisely determined the gene structures and positions of the transcriptional start sites, which are indispensable for the identification of the promoter regions. (iii) A total of 4257 cDNA sequences were newly generated from murine malaria parasites, Plasmodium yoelii yoelii. The genome/cDNA sequences were compared at both nucleotide and amino acid levels, with those of P.falciparum, and the sequence alignment for each gene is presented graphically. This part of the database serves as a versatile platform to elucidate the function(s) of malaria genes by a comparative genomic approach. It should also be noted that all of the cDNAs represented in this database are supported by physical cDNA clones, which are publicly and freely available, and should serve as indispensable resources to explore functional analyses of malaria genomes.
全疟原虫数据库(http://fullmal.ims.u-tokyo.ac.jp),一个来自人类疟原虫恶性疟原虫的全长cDNA数据库,已在至少三个方面进行了更新。(i)我们添加了从新文库中生成的8934个序列,使我们的11424个全长cDNA集合覆盖了估计的5409个寄生虫基因总数中的1375个(25%)。(ii)我们所有的全长cDNA和GenBank EST序列与公开可用的注释基因和其他预测一起被映射到基因组序列上。这精确地确定了基因结构和转录起始位点的位置,这对于启动子区域的识别是必不可少的。(iii)总共从鼠疟原虫约氏疟原虫中生成了4257个新的cDNA序列。在核苷酸和氨基酸水平上,将基因组/cDNA序列与恶性疟原虫的序列进行了比较,并以图形方式展示了每个基因的序列比对。数据库的这一部分作为一个通用平台,通过比较基因组方法阐明疟疾基因的功能。还应注意的是,该数据库中所有代表的cDNA都有物理cDNA克隆的支持,这些克隆是公开免费提供的,应作为探索疟疾基因组功能分析的不可或缺的资源。