Lugert T, Werr W
Institut für Genetik der Universität zu Köln, Germany.
Plant Mol Biol. 1994 Jun;25(3):493-506. doi: 10.1007/BF00043877.
South-western screening of lambda gt11 expression library with a fragment of the Shrunken promoter containing the initiator element resulted in cloning of a novel maize gene. The encoded initiator-binding protein (IBP1) interacts at the transcription start site of the Shrunken promoter. Analysis of the 680 amino acid (aa) long polypeptide revealed a novel bipartite DNA-binding domain at the carboxyl terminus. In its amino-terminal part, it is weakly related to Myb R-repeats but the following basic region is also essential for DNA binding. A region of similarity to the conserved 2.1 and 2.2 motifs in bacterial sigma-factors is located close to the IBP1 amino terminus. Two putative nuclear localization signals are compatible with the presence of antigenically related polypeptides in nuclear protein extracts. The IBP1 gene was mapped to the long arm of chromosome 9 (9L095); a second highly related gene IBP2 is located on the short arm of chromosome 1 (1S014). Both genes encode proteins sharing 93% similarity and are transcribed with similar activity in different plant organs. A small 82 nucleotide intron in the IBP2 transcript is found unspliced to a variable degree in different tissues. Translation of this incompletely processed transcript would result in a truncated amino-terminal polypeptide lacking the DNA-binding domain.
用含有起始元件的皱缩基因启动子片段对λgt11表达文库进行西南杂交筛选,从而克隆出一个新的玉米基因。所编码的起始子结合蛋白(IBP1)在皱缩基因启动子的转录起始位点相互作用。对这条680个氨基酸长的多肽进行分析,结果显示在其羧基末端有一个新的双功能DNA结合结构域。在其氨基末端部分,它与Myb R重复序列有微弱的相关性,但随后的碱性区域对DNA结合也至关重要。一个与细菌σ因子中保守的2.1和2.2基序相似的区域位于靠近IBP1氨基末端的位置。两个推定的核定位信号与核蛋白提取物中存在抗原相关多肽的情况相符。IBP1基因被定位到9号染色体的长臂(9L095);另一个高度相关的基因IBP2位于1号染色体的短臂(1S014)。这两个基因编码的蛋白质有93%的相似性,并且在不同植物器官中的转录活性相似。在IBP2转录本中发现一个82个核苷酸的小内含子,在不同组织中其剪接程度不同。这种未完全加工的转录本的翻译将产生一个缺少DNA结合结构域的截短的氨基末端多肽。