DeZazzo J D, Falck-Pedersen E, Imperiale M J
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109-0620.
Mol Cell Biol. 1991 Dec;11(12):5977-84. doi: 10.1128/mcb.11.12.5977-5984.1991.
Temporal regulation of poly(A) site choice occurs in an adenovirus recombinant encoding a miniature version of the major late transcription unit with two poly(A) sites, L1 and L3. Using deletion mutagenesis, we have looked directly for cis-acting elements regulating poly(A) site choice in this recombinant. From this work, we draw two main conclusions. First, elements other than the AAUAAA and downstream sequences of the L1 poly(A) site are required for temporal regulation of poly(A) site choice during infection. Second, these regions function in two distinct modes during infection. The two regions enhance selection of the L1 poly(A) site in an additive manner during an early infection, but deletion of either element abolishes the switch in poly(A) site choice during a late infection. This work documents the first example of a regulatory element downstream of a core poly(A) region.
在一个编码主要晚期转录单元微型版本且带有两个聚腺苷酸化(poly(A))位点L1和L3的腺病毒重组体中,发生了聚(A)位点选择的时间调控。利用缺失诱变,我们直接寻找在此重组体中调控聚(A)位点选择的顺式作用元件。从这项工作中,我们得出两个主要结论。第一,在感染期间聚(A)位点选择的时间调控需要L1聚(A)位点的AAUAAA和下游序列以外的元件。第二,这些区域在感染期间以两种不同模式发挥作用。在早期感染期间,这两个区域以累加方式增强L1聚(A)位点的选择,但在晚期感染期间,删除任何一个元件都会消除聚(A)位点选择的转换。这项工作记录了核心聚(A)区域下游调控元件的首个实例。