Gasser S M, Laemmli U K
Cell. 1986 Aug 15;46(4):521-30. doi: 10.1016/0092-8674(86)90877-9.
We find DNA fragments attached to the nuclear scaffold (SARs) both 5' and 3' of three Drosophila genes, defining looped domains ranging from 4.5 to 13 kb. For the two-promoter-containing gene Adh (alcohol dehydrogenase), we find two upstream and two downstream SARs. For Sgs-4, the 5' SAR covers 866 bp immediately upstream of the transcript, and in the case of fushi tarazu, the 5' SAR is found on a small fragment 4.8 kb upstream of the start of transcription. These four upstream scaffold-attached fragments comap with enhancer-like regulatory sequences. Sequence analysis of five upstream SARs reveals clusters of sequences closely related to the cleavage consensus of topoisomerase II, several copies of a specific 10 bp A-rich sequence (AATAAATCAAA), and another 10 bp T-rich stretch.
我们在三个果蝇基因的5'端和3'端均发现了附着于核支架(SARs)的DNA片段,这些片段界定了范围从4.5至13 kb的环状结构域。对于含有两个启动子的基因Adh(乙醇脱氢酶),我们发现了两个上游和两个下游SARs。对于Sgs-4基因,5'端的SAR覆盖了转录本上游紧邻的866 bp区域;而对于ftz(分节基因)基因,5'端的SAR位于转录起始点上游4.8 kb的一个小片段上。这四个上游附着于支架的片段与增强子样调控序列共定位。对五个上游SARs的序列分析揭示了与拓扑异构酶II切割共有序列密切相关的序列簇、特定的富含A的10 bp序列(AATAAATCAAA)的多个拷贝以及另一个富含T的10 bp片段。