水稻半矮化基因sd-1的定位克隆:水稻“绿色革命基因”编码一种参与赤霉素合成的突变酶。

L. Monna, Noriyuki Kitazawa, R. Yoshino, Junko Suzuki, Haruka Masuda, Y. Maehara, M. Tanji, Mizuho Sato, S. Nasu, Y. Minobe
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引用次数: 454

摘要

被称为“绿色革命基因”的水稻半矮化基因sd-1通过定位克隆被分离出来,并被发现编码赤霉素生物合成途径的关键酶赤霉素20氧化酶。使用几种基于pcr的标记技术(包括cleaved扩增多态性序列、derived-CAPS和单核苷酸多态性)对3477个分离片段进行分析,发现在6 kb候选区间内存在1个ORF。正常型水稻在该区域具有相同的序列,包括3个外显子(558、318和291 bp)和2个内含子(105和1471 bp)。dee - geo - woogen型sd-1突变体从1号外显子中间到2号外显子上游,基因组中有383-bp的缺失(表达序列中有278-bp的缺失),包括一个105-bp的内含子,导致帧移位,在缺失位点后产生终止密码子。辐射诱导的sd-1突变体Calrose 76外显子2有一个1 bp的替换,导致氨基酸替换(Leu [CTC]到Phe [TTC])。表达分析表明,在sd-1突变体中至少存在一个多位点的赤霉素20-氧化酶,这可能阻止了严重侏儒症的发生。
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Positional cloning of rice semidwarfing gene, sd-1: rice "green revolution gene" encodes a mutant enzyme involved in gibberellin synthesis.
A rice semidwarfing gene, sd-1, known as the "green revolution gene," was isolated by positional cloning and revealed to encode gibberellin 20-oxidase, the key enzyme in the gibberellin biosynthesis pathway. Analysis of 3477 segregants using several PCR-based marker technologies, including cleaved amplified polymorphic sequence, derived-CAPS, and single nucleotide polymorphisms revealed 1 ORF in a 6-kb candidate interval. Normal-type rice cultivars have an identical sequence in this region, consisting of 3 exons (558, 318, and 291 bp) and 2 introns (105 and 1471 bp). Dee-Geo-Woo-Gen-type sd-1 mutants have a 383-bp deletion from the genome (278-bp deletion from the expressed sequence), from the middle of exon 1 to upstream of exon 2, including a 105-bp intron, resulting in a frame-shift that produces a termination codon after the deletion site. The radiation-induced sd-1 mutant Calrose 76 has a 1-bp substitution in exon 2, causing an amino acid substitution (Leu [CTC] to Phe [TTC]). Expression analysis suggests the existence of at least one more locus of gibberellin 20-oxidase which may prevent severe dwarfism from developing in sd-1 mutants.
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