Waldron C, Wills N, Gesteland R F
J Mol Appl Genet. 1985;3(1):7-17.
We have identified cloned fragments of the soybean genome that hybridize to total soybean tRNA. Five of these clones, chosen at random, have unique patterns of restriction endonuclease sites and contain only a small region that is homologous to tRNA (less than 1 kb of 10-12 kb cloned). Two of the hybridizing fragments were subcloned and regions of about 600 bp including the homologies were sequenced. Each region contains a single putative tRNA gene, for tRNAasp or tRNAmet, surrounded by DNA rich in AT basepairs (68-82%). Neither sequence encodes the amino acid-accepting -CCA terminus. The tRNAasp gene does not contain any intervening sequences, but the tRNAmet gene has an 11-bp sequence in the anticodon loop that would not be expected in the mature tRNA. There appear to be a small number of sequences within the soybean genome that share homology with each of the regions containing a putative tRNA gene.
我们已经鉴定出大豆基因组中与大豆总tRNA杂交的克隆片段。随机选择的其中5个克隆具有独特的限制性内切酶位点模式,并且仅包含一个与tRNA同源的小区域(在10 - 12 kb的克隆片段中小于1 kb)。将两个杂交片段进行亚克隆,并对包括同源性区域在内的约600 bp区域进行测序。每个区域都包含一个单一的推定tRNA基因,分别为天冬氨酸tRNA或甲硫氨酸tRNA,其周围是富含AT碱基对(68 - 82%)的DNA。两个序列均未编码氨基酸接受 -CCA末端。天冬氨酸tRNA基因不包含任何间隔序列,但甲硫氨酸tRNA基因在反密码子环中有一个11 bp的序列,这在成熟tRNA中是不会出现的。大豆基因组中似乎有少量序列与每个包含推定tRNA基因的区域具有同源性。