Schaeffer L, Roy R, Humbert S, Moncollin V, Vermeulen W, Hoeijmakers J H, Chambon P, Egly J M
UPR 6520 (CNRS), Unité 184 (INSERM), Faculté de Médecine, Strasbourg, France.
Science. 1993 Apr 2;260(5104):58-63. doi: 10.1126/science.8465201.
The human BTF2 basic transcription factor (also called TFIIH), which is similar to the delta factor in rat and factor b in yeast, is required for class II gene transcription. A strand displacement assay was used to show that highly purified preparation of BTF2 had an adenosine triphosphate-dependent DNA helicase activity, in addition to the previously characterized carboxyl-terminal domain kinase activity. Amino acid sequence analysis of the tryptic digest generated from the 89-kilodalton subunit of BTF2 indicated that this polypeptide corresponded to the ERCC-3 gene product, a presumed helicase implicated in the human DNA excision repair disorders xeroderma pigmentosum and Cockayne's syndrome. These findings suggest that transcription and nucleotide excision repair may share common factors and hence may be considered to be functionally related.
人类BTF2基本转录因子(也称为TFIIH),类似于大鼠中的δ因子和酵母中的b因子,是II类基因转录所必需的。采用链置换分析表明,高度纯化的BTF2制剂除了先前已鉴定的羧基末端结构域激酶活性外,还具有依赖三磷酸腺苷的DNA解旋酶活性。对从BTF2的89千道尔顿亚基产生的胰蛋白酶消化产物进行氨基酸序列分析表明,该多肽对应于ERCC-3基因产物,一种推测的解旋酶,与人类DNA切除修复疾病色素性干皮病和科凯恩综合征有关。这些发现表明转录和核苷酸切除修复可能共享共同因子,因此可被认为在功能上相关。