Young R J, Francis D M, St Clair D A, Taylor B H
Department of Biology, Texas A & M University, College Station 77843-3258.
Genetics. 1994 Jun;137(2):581-8. doi: 10.1093/genetics/137.2.581.
A segment of DNA 5' to the transcribed region of an auxin-regulated gene, ARPI, from Lycopersicon esculentum Mill. cv. VFN8 contains a sequence with the structural characteristics of a transposable element. The putative element (Lyt1) is 1340 bp long, has terminal inverted repeats of approximately 235 bp and is flanked by 9-bp direct repeats. Lyt1 has a structure similar to the Robertson's Mutator (Mu) family from maize. The terminal inverted repeats are 80% AT-rich, are 96.6% identical, and define a larger family of repetitive elements. Southern analysis and genomic dot-blot reconstructions detected at least 41 copies of Lyt1-hybridizing sequences in red-fruited Lycopersicon spp. (L. esculentum, L. pimpinellifolium and L. cheesmanii), and 2-8 copies in the green-fruited species (L. hirsutum, L. pennellii, L. peruvianum, L. chilense and L. chmielewskii). There were two to four copies in the Solanum spp. closely allied with the genus Lycopersicon (S. lycopersicoides, S. ochranthum and S. juglandifolium), while the more distantly related Solanum spp. showed little (one to two copies in S. tuberosum) to no (S. quitoense) detectable hybridization under stringent conditions. Linkage analysis in the F2 progeny of a cross between L. esculentum and L. cheesmanii indicated that at least six loci that hybridize to the Lyt1 sequence are dispersed in the genome. Polymerase chain reaction and Southern analyses revealed that some red-fruited accessions and L. chmielewskii lacked Lyt1 5' to the transcribed region of ARPI. Subsequent sequence analysis indicated that only one copy of the 9-bp direct repeat (target site) was present, suggesting that transposition of the element into the ARPI gene occurred after the divergence of the red-fruited and green-fruited Lycopersicon species.
来自番茄(Lycopersicon esculentum Mill. cv. VFN8)生长素调节基因ARPI转录区域5'端的一段DNA含有一个具有转座元件结构特征的序列。推测的元件(Lyt1)长度为1340 bp,具有约235 bp的末端反向重复序列,两侧为9 bp的正向重复序列。Lyt1的结构类似于玉米的罗伯逊突变体(Mu)家族。末端反向重复序列富含80%的AT,96.6%相同,并定义了一个更大的重复元件家族。Southern分析和基因组斑点杂交重建在红果番茄属物种(番茄、醋栗番茄和契斯曼尼番茄)中检测到至少41个与Lyt1杂交的序列拷贝,在绿果物种(多毛番茄、潘那利番茄、秘鲁番茄、智利番茄和奇美留斯基番茄)中检测到2 - 8个拷贝。与番茄属密切相关的茄属物种(番茄叶型茄、黄果茄和胡桃叶茄)中有2至4个拷贝,而亲缘关系较远的茄属物种在严格条件下显示出很少(马铃薯中有1至2个拷贝)到没有(基多茄)可检测到的杂交信号。番茄和契斯曼尼番茄杂交的F2后代的连锁分析表明,至少有6个与Lyt1序列杂交的位点分散在基因组中。聚合酶链反应和Southern分析表明,一些红果种质和奇美留斯基番茄在ARPI转录区域5'端缺少Lyt1。随后的序列分析表明,仅存在一个9 bp正向重复序列(靶位点)拷贝,这表明该元件向ARPI基因的转座发生在红果和绿果番茄物种分化之后。