Esch J J, Oppenheimer D G, Marks M D
School of Biological Sciences, University of Nebraska-Lincoln, NE 68588-0118.
Plant Mol Biol. 1994 Jan;24(1):203-7. doi: 10.1007/BF00040586.
A genomic clone containing the gl1-2 allele has been isolated and sequenced. The predicted amino acid sequence of the gl1-2 protein is identical to that of the GL1-Col allele up to position 201. At this point in the coding region of gl1-2 there is a deletion relative to the wild-type sequence that results in an in-frame stop codon at position 202. This deletion removes 27 amino acid residues, including a highly negatively charged region, from the predicted gl1-2 polypeptide. The loss of this negatively charged carboxy-terminal region from the gl1-2 product is most likely the cause of the partial loss of gene activity which results in a reduction in leaf trichome initiation.
一个包含gl1-2等位基因的基因组克隆已被分离并测序。gl1-2蛋白的预测氨基酸序列在第201位之前与GL1-Col等位基因的序列相同。在gl1-2的编码区域的这一点上,相对于野生型序列存在一个缺失,该缺失导致在第202位出现一个框内终止密码子。这个缺失从预测的gl1-2多肽中去除了27个氨基酸残基,包括一个高度带负电荷的区域。gl1-2产物中这个带负电荷的羧基末端区域的缺失很可能是基因活性部分丧失的原因,而基因活性丧失导致叶毛起始减少。