Taylor L P, Walbot V
EMBO J. 1985 Apr;4(4):869-76. doi: 10.1002/j.1460-2075.1985.tb03712.x.
Insertion of the maize transposable element Mu-1 into the first intron of the alcohol dehydrogenase locus (Adh1) of maize produced mutant Adh1-S3034 with 40% of the wild-type level of protein and mRNA. Continued instability at this locus resulted in secondary mutations with lower levels of protein expression. One of these, Adh1-S3034a, has no detectable ADH1 expression. This paper describes the precise nature of the changes in the Adh1 gene that gave rise to the S3034a allele. The Mu-1 element is still present in the mutant, but Adh1 sequences immediately adjacent to the element are deleted. The deletion starts precisely at the Mu-1 insertion site and extends 74 bp leftward removing part of the first intron, the intron:exon junction and 2 bp of the eleventh amino acid codon in the first exon of the gene. Tests for reversion within the somatic tissue of plants show that mutant S3034a, unlike its progenitor, is stably null for ADH1 activity.
将玉米转座因子Mu-1插入玉米乙醇脱氢酶基因座(Adh1)的第一个内含子中,产生了突变体Adh1-S3034,其蛋白质和mRNA水平为野生型水平的40%。该基因座的持续不稳定性导致了蛋白质表达水平较低的二次突变。其中之一,Adh1-S3034a,没有可检测到的ADH1表达。本文描述了导致S3034a等位基因的Adh1基因变化的确切性质。Mu-1元件仍存在于突变体中,但与该元件紧邻的Adh1序列被删除。缺失恰好从Mu-1插入位点开始,并向左延伸74 bp,去除了第一个内含子的一部分、内含子与外显子的交界处以及该基因第一个外显子中第11个氨基酸密码子的2个碱基对。对植物体细胞组织内回复突变的测试表明,突变体S3034a与其亲本不同,其ADH1活性稳定地缺失。