Sollitti P, Marmur J
Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461.
Mol Gen Genet. 1988 Jul;213(1):56-62. doi: 10.1007/BF00333398.
We determined the complete nucleotide sequence of the yeast MAL6R gene from the Saccharomyces carlsbergensis MAL6 locus. The MAL6R gene encodes a transacting protein required for the inducible, coordinate expression of the two divergently transcribed structural genes, MAL6T (maltose permease), and MAL6S (maltase) at this locus. The transcription initiation sites for MAL6R were determined by primer extension experiments. The MAL6R gene contains an open reading frame of 473 amino acids with a calculated Mr of 54,892. The N-terminus of the deduced protein contains an amino acid sequence isologous to a consensus sequence for cysteine-zinc associated DNA binding fingers found in other fungal DNA binding proteins. The MAL6R gene was mapped to chromosome VIII by using OFAGE (orthagonal field alternating gel electrophoresis) gels and hybridization with specific chromosome and MAL6 probes.
我们测定了来自卡尔斯伯酵母MAL6位点的酵母MAL6R基因的完整核苷酸序列。MAL6R基因编码一种反式作用蛋白,该蛋白是在此位点诱导性、协同表达两个反向转录的结构基因MAL6T(麦芽糖通透酶)和MAL6S(麦芽糖酶)所必需的。通过引物延伸实验确定了MAL6R的转录起始位点。MAL6R基因包含一个473个氨基酸的开放阅读框,计算出的分子量为54,892。推导蛋白的N端包含一段氨基酸序列,该序列与在其他真菌DNA结合蛋白中发现的半胱氨酸-锌相关DNA结合指的共有序列同源。通过使用正交场交变凝胶电泳(OFAGE)凝胶以及与特定染色体和MAL6探针杂交,将MAL6R基因定位到第八条染色体上。