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玉米花青素调控位点C1的分子分析

Molecular analysis of the maize anthocyanin regulatory locus C1.

作者信息

Cone K C, Burr F A, Burr B

出版信息

Proc Natl Acad Sci U S A. 1986 Dec;83(24):9631-5. doi: 10.1073/pnas.83.24.9631.

DOI:10.1073/pnas.83.24.9631
PMID:3025847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC387194/
Abstract

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.

摘要

玉米的C1基因在胚乳糊粉层花青素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的一个可突变等位基因c1-m5来实现的,该等位基因含有转座因子Spm。分子和遗传分析相结合,用于鉴定C1位点处的Spm。用甲基敏感限制性酶消化来自c1可突变表型与隐性c1表型分离群体的个体基因组DNA,并用源自缺陷型Spm的小DNA片段进行探测。与Spm探针互补的一个Sal I限制性片段在具有c1-m5表型的个体DNA中存在,但在具有隐性c1表型的个体DNA中不存在。随后对该片段进行克隆和限制性分析,揭示了Spm侧翼的序列,这些序列被证明是C1特异性的。然后将源自侧翼序列的DNA片段用作探针,克隆野生型C1基因和C1的几个其他等位基因,包括一个稳定的隐性等位基因、两个由Ds插入引起的突变、一个由缺陷型Spm插入诱导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,C1在花青素生物合成途径中对Bz1和A1结构基因的调控是在转录水平上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/9cd2d7321eb6/pnas00328-0369-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/d80e2ff030b0/pnas00328-0367-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/496228cb04fe/pnas00328-0368-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/40636e99c396/pnas00328-0369-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/a9c602c6d32c/pnas00328-0369-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/9cd2d7321eb6/pnas00328-0369-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/d80e2ff030b0/pnas00328-0367-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/496228cb04fe/pnas00328-0368-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/40636e99c396/pnas00328-0369-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/a9c602c6d32c/pnas00328-0369-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/751d/387194/9cd2d7321eb6/pnas00328-0369-c.jpg

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