Hahn S, Kruse U, Rüger W
Nucleic Acids Res. 1986 Dec 9;14(23):9311-27. doi: 10.1093/nar/14.23.9311.
The product of gene 33 is essential for the regulation of late transcription and gene product 59 is required in recombination, DNA repair and replication. The exact functions of both proteins are not known. Restriction fragments spanning the genomic area of genes 33 and 59 have been cloned into phage M13 and a 4.9 kb nucleotide sequence has been determined. Translation of the DNA sequence predicted that gp33 contains 112 amino acids with a mol.wt. of 12.816 kd while gp59 is composed of 217 amino acids adding up to a mol.wt. of 25.967 kd. The genomic area studied here also contains 3 open reading frames of genes not identified to date and it is thought to include the NH2-terminal part of g34. One of the open reading frames seems to code for the 10 kd protein, probably involved in the regulation of transcription of bacteriophage T4. This protein is predicted to consist of 89 amino acid residues with a mol.wt. of 10.376 kd. Gene 33 and the gene for the 10 kd protein were cloned separately on high expression vectors resulting in over-production of the two proteins.
基因33的产物对于晚期转录的调控至关重要,而基因产物59在重组、DNA修复和复制过程中是必需的。这两种蛋白质的确切功能尚不清楚。跨越基因33和59基因组区域的限制性片段已被克隆到噬菌体M13中,并且已经确定了一段4.9 kb的核苷酸序列。对该DNA序列的翻译预测,gp33含有112个氨基酸,分子量为12.816 kd,而gp59由217个氨基酸组成,分子量总计为25.967 kd。此处研究的基因组区域还包含3个迄今尚未鉴定的基因的开放阅读框,并且认为它包括g34的NH2末端部分。其中一个开放阅读框似乎编码10 kd的蛋白质,可能参与噬菌体T4转录的调控。预测该蛋白质由89个氨基酸残基组成,分子量为10.376 kd。基因33和10 kd蛋白质的基因分别克隆到高表达载体上,导致这两种蛋白质过量产生。