【2h】

Molecular analysis of the maize anthocyanin regulatory locus C1.

机译:玉米花色苷调节位点C1的分子分析。

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摘要

The C1 gene of maize plays a regulatory role in the production of anthocyanin pigments in the aleurone layer of the endosperm. As an initial step toward understanding the molecular details of how C1 controls pigment biosynthesis, we cloned the C1 gene. This was accomplished by first cloning a mutable allele of C1, c1-m5, which contains the transposable element Spm. A combination of molecular and genetic analysis was used to identify the Spm at the C1 locus. Individual genomic DNAs from a population in which the c1-mutable phenotype was segregating with the recessive c1 phenotype were digested with methyl-sensitive restriction enzymes and probed with a small DNA fragment derived from a defective Spm. One Sal I restriction fragment complementary to the Spm probe was shown to be present in the DNA of individuals with the c1-m5 phenotype but absent from DNA of individuals with a recessive c1 phenotype. Subsequent cloning and restriction analysis of this fragment revealed sequences flanking the Spm that proved to be C1-specific. A DNA fragment derived from the flanking sequences was then used as a probe to clone the wild-type C1 gene and several additional alleles of C1, including one stable recessive, two mutations caused by Ds insertions, one mutation induced by insertion of a defective Spm, and two dominant mutations, C1-S and C1-I. RNA blot hybridization analysis of three C1 alleles indicates that C1 regulation of the Bz1 and A1 structural genes in the anthocyanin biosynthetic pathway is at the transcriptional level.
机译:玉米的C1基因在胚乳糊粉层中花色苷色素的产生中起调节作用。作为了解C1如何控制色素生物合成的分子细节的第一步,我们克隆了C1基因。这是通过首先克隆C1的可变等位基因c1-m5来实现的,其中包含转座因子Spm。分子分析和遗传分析相结合,用于鉴定C1位点的Spm。用甲基敏感的限制性内切酶消化c1可变表型与隐性c1表型隔离的群体的单个基因组DNA,并用衍生自缺陷性Spm的小DNA片段进行探测。已显示与Spm探针互补的一个Sal I限制性片段存在于具有c1-m5表型的个体的DNA中,但不存在于具有隐性c1表型的个体的DNA中。随后对该片段的克隆和限制性酶切分析揭示了Spm侧翼的序列,该序列被证明具有C1特异性。然后,将来自侧翼序列的DNA片段用作探针,以克隆野生型C1基因和C1的其他几个等位基因,包括一个稳定的隐性,两个由Ds插入引起的突变,一个由有缺陷的Spm插入引起的突变。 ,以及两个显性突变C1-S和C1-I。对三个C1等位基因的RNA印迹杂交分析表明,花色苷生物合成途径中Bz1和A1结构基因的C1调控处于转录水平。

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