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Complementation of methylation deficiency in embryonic stem cells by a DNA methyltransferase minigene

机译:DNA甲基转移酶小基因对胚胎干细胞中甲基化缺陷的补充

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摘要

Previous attempts to express functional DNA cytosine methyltransferase (EC 2.1.1.37) in cells transfected with the available Dnmt cDNAs have met with little or no success. We show that the published Dnmt sequence encodes an amino terminal-truncated protein that is tolerated only at very low levels when stably expressed in embryonic stem cells. Normal expression levels were, however, obtained with con- structs containing a continuation of an ORF with a coding capacity of up to 171 amino acids upstream of the previously defined start site. The protein encoded by these constructs comigrated in SDS/PAGE with the endogenous enzyme and restored methylation activity in transfected cells.
机译:先前尝试在用可用Dnmt cDNA转染的细胞中表达功能性DNA胞嘧啶甲基转移酶(EC 2.1.1.37)的尝试很少成功,甚至没有成功。我们表明,已发布的Dnmt序列编码在胚胎干细胞中稳定表达时仅能以非常低的水平耐受的氨基末端截短蛋白。但是,正常表达水平是通过含有ORF连续序列的结构获得的,该序列的编码能力在先前定义的起始位点上游最多包含171个氨基酸。这些构建体编码的蛋白质在SDS / PAGE中与内源酶竞争,并在转染的细胞中恢复了甲基化活性。

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