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Distribution and characterization of more than 1000 T-DNA tags in the genome of Brachypodium distachyon community standard line Bd21

机译:在BroChymodium distachyon社区标准线BD21的基因组中分布和表征超过1000吨DNA标签

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A collection of 4117 fertile T-DNA lines has been generated by Agrobacterium-mediated transformation of the diploid community standard line Bd21 of Brachypodium distachyon. The regions flanking the T-DNA left and right borders of the first 741 transformed plants were isolated by adapter-ligation PCR and sequenced. A total of 1005 genomic sequences (representing 44.1% of all flanking sequences retrieved) characterized 660 independent T-DNA loci assigned to a unique location in the Brachypodium genome sequence. Seventy-six percent of the fertile plant lines contained at least one anchored T-DNA locus (1.17 loci per tagged line on average). Analysis of the regions flanking both borders of the T-DNA increased the number of T-DNA loci tagged and the number of tagged lines by approximately 50% when compared to a single border analysis. T-DNA integration (2.4 insertions per Mb on average) was proportional to chromosome size, however, varied greatly along each chromosome with often low insertion level around centromeres. The frequency of insertion within transposable elements (5.3%) was fivefold lower than expected if random insertion would have occurred. More than half of the T-DNAs inserted in genic regions. On average, one gene could be tagged for every second fertile plant line produced and more than one plant line out of three contained a T-DNA insertion directly within or 500 bp around the coding sequence. Approximately, 60% of the genes tagged corresponded to expressed genes. The T-DNA lines generated by the BrachyTAG programme are available as a community resource and have been distributed internationally since 2008 via the BrachyTAG.org web site.
机译:通过农杆菌介导的二倍体群体标准线BD21的T-DNA系列产生了4117种肥沃的T-DNA系列的集合。侧翼的区域由Adapter-Catization PCR分离出第一741转化的植物的T-DNA左和右边边界并测序。总共1005个基因组序列(代表检索的所有侧翼序列的44.1%)表征了分配到铜卷曲基因组序列中的独特位置的660个独立的T-DNA基因座。百分之六六个肥沃的植物系含有至少一个锚定T-DNA基因座(平均标记线的1.17个基因座)。与单一边界分析相比,T-DNA的两个边界的分析增加了T-DNA的两个边界,增加了T-DNA基因座的数量和标记线的数量约50%。 T-DNA积分(平均每MB的2.4插入)与染色体尺寸成比例,然而,沿着每种染色体大大变化,通常在焦粒周围的插入水平低。如果发生随机插入,可转换元件(5.3%)内的插入频率为低于预期的五倍。在遗传区域中插入的超过一半T-DNA。平均而言,可以针对产生的每种第二次肥沃的植物管线标记一个基因,并且三种植物排出的植物线在编码序列周围直接含有T-DNA插入或500bp。大约,标记的60%的基因对应于表达的基因。 BrachyTag程序生成的T-DNA线作为社区资源可用,自2008年以来通过BRACHYTAG.ORG网站在国际上进行。

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