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DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus

机译:啤酒酵母2微米质粒STB位点分配能力所需的DNA序列元件

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摘要

Equal partitioning of the multi-copy yeast 2-micron plasmid requires association of plasmid proteins Rep1 and Rep2 with tandem repeats at the plasmid STB locus. To identify sequence elements required for these associations we generated synthetic versions of a 63-bp section of STB, encompassing one repeat. A single copy of this sequence was sufficient for Rep protein association in vivo, while two directly arrayed copies provided partitioning function to a plasmid lacking all other 2-micron sequences. Partitioning efficiency increased with increasing repeat number, reaching that conferred by the native STB repeat array. By altering sequences in synthetic repeats, we identified the TGCA component of a TGCATTTTT motif as critical for Rep protein recognition, with a second TGCA sequence in each repeat also contributing to association. Mutation of TGCATTTTT to TGTATTTT, as found in variant 2-micron STB repeats, also allowed Rep protein association, while mutation to TGCATTAAT impaired inheritance without abolishing Rep protein recognition, suggesting an alternate role for the T-tract. Our identification of sequence motifs required for Rep protein recognition provides the basis for understanding higher-order Rep protein arrangements at STB that enable the yeast 2-micron plasmid to be efficiently partitioned during host cell division.
机译:多拷贝酵母2微米质粒的均等分配要求质粒蛋白Rep1和Rep2与质粒STB位点的串联重复序列相关联。为了鉴定这些关联所需的序列元件,我们生成了STB的63 bp部分的合成版本,包括一个重复。该序列的单个拷贝足以在体内与Rep蛋白缔合,而两个直接排列的拷贝为缺乏所有其他2微米序列的质粒提供了分配功能。分区效率随着重复次数的增加而增加,达到了本机STB重复数组所赋予的效率。通过更改合成重复序列中的序列,我们确定了TGCATTTTT基序的TGCA成分对于Rep蛋白的识别至关重要,每个重复序列中的第二个TGCA序列也有助于缔合。 TGCATTTTT突变为TGTATTTT(在2微米STB重复序列中发现)也允许Rep蛋白缔合,而TGCATTAAT突变则在不破坏Rep蛋白识别的情况下损害了遗传,暗示了T通道的另一种作用。我们对Rep蛋白识别所需的序列基序的鉴定为理解STB上的高级Rep蛋白排列提供了基础,该排列使酵母2微米质粒在宿主细胞分裂过程中得以有效分配。

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