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Retrotransposons of rice as a tool for the functional analysis of genes

机译:水稻重转渣作为基因功能分析的工具

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Five endogenous active retrotransposons have been found in rice. Among them, the most active one, called Tos17, was characterized in detail. Tos17 is silent under-normal conditions and becomes active only under tissue culture conditions. Five to 30transposed Tos17 copies were found in each plant regenerated from culture. Tos17 was shown to transpose preferentially into low-copy-number, gene-rich regions, indicating that Tos17 can be used as an efficient insertional mutagen. A collection of 32,000regenerated rice lines carrying about 256,000 insertions was generated, and these lines are being used for forward and reverse genetic analyses. By using a transposon-tagging strategy, causative genes for viviparous, dwarf, semidwarf, brittle culm, palegreen, and narrow leaf mutations, among others, have been cloned. For reverse genetic studies, two strategies are being employed. One is the polymerase chain reaction (PCR) screening of mutants of the gene of interest. We screened 12,000 lines and foundmutants of 15 genes, including MAPK, MADS-box, and P450 genes, among the 47 genes analyzed. This suggests that at least 37,000 lines are required for saturation mutagenesis. Another important strategy is the random sequencing of mutated genes by isolating the sequences flanking transposed Tos17. The flanking sequences are amplified by TAlL (thermal asymmetric interlaced)- and suppression-PCR and directly sequenced. Until now, 7,376 independent flanking sequences from 2,134 lines have been determined andmutants of different classes of genes have been identified.
机译:在米饭中发现了五个内源性活性反向转化渣。其中,详细描述了称为TOS17的最活跃的一个。 TOS17是沉默的正常条件下,仅在组织培养条件下变得活跃。在从培养中再生的每株植物中发现了五到30份TOS17副本。显示TOS17优先转化为低拷贝数,富含基因的区域,表明TOS17可以用作有效的插入诱变。产生32,000℃的32,000重新加入稻米的系列,这些系列用于前进和反向遗传分析。通过使用转座子标记策略,克隆了viviparous,矮化,半糖,脆弱枯枝杆菌,古格和窄叶突变的致病基因。对于逆向遗传研究,正在使用两种策略。一种是感兴趣基因突变体的聚合酶链反应(PCR)筛选。在分析的47个基因中,我们筛选了15个基因的12,000条线和牧场,包括Mapk,Mads-Box和P450基因。这表明饱和诱变需要至少37,000条线。另一种重要的策略是通过隔离翻转TO17的序列来随机测序突变基因。侧翼序列通过高(热不对称互通)和抑制-PCR扩增并直接测序。到目前为止,已经确定了来自2,134系的7,376个独立的侧翼序列,并确定了不同类别的基因的沉淀。

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