Costeas P A, Chinsky J M
Department of Pediatrics, University of Maryland School of Medicine, Baltimore 21201, USA.
Biochim Biophys Acta. 1998 Jul 30;1399(1):111-6. doi: 10.1016/s0167-4781(98)00084-0.
The promoter region of the murine branched-chain alpha-ketoacid dehydrogenase E2 subunit (dihydrolipoyl transacylase) gene was isolated and characterized. Sequence analysis of the promoter-regulatory region showed the presence of two inverted 'CAAT box' sequences, the most proximal being -42 to -48 bp upstream from the determined transcription initiation site, but no TATA-box sequences, similar to the human BCKAD E2 gene. The boundary of the minimum promoter sequence appeared to reside just inclusive of this first inverted CAAT sequence, but minigene transfer analysis demonstrated that the promoter proximal between -65 and -140 bp is likely to be extremely important for controlling regulated changes in E2 RNA expression. The regulatory effect of this region may be modulated by a number of other upstream regions which were identified within the 7.0 kb sequence examined.
小鼠支链α-酮酸脱氢酶E2亚基(二氢硫辛酰胺转乙酰基酶)基因的启动子区域被分离并进行了特征分析。对启动子调控区域的序列分析显示存在两个反向的“CAAT盒”序列,最靠近的一个位于确定的转录起始位点上游-42至-48碱基对处,但没有TATA盒序列,这与人类BCKAD E2基因相似。最小启动子序列的边界似乎刚好包含第一个反向CAAT序列,但微型基因转移分析表明,-65至-140碱基对之间的启动子近端区域对于控制E2 RNA表达的调节变化可能极其重要。该区域的调节作用可能受到在所检测的7.0 kb序列内鉴定出的许多其他上游区域的调节。