The induction of dominant somatic mutations at the Dlb-1 locus

Lidia Cosentino, John A. Heddle
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引用次数: 7

Abstract

In the small intestine of heterozygous mice (Dlb-1b/Dlba), the Dlb-1 allele results in a stainable epithelium. The mutation or loss of the dominant Dlb-1b allele in a stem cell results in a non-staining ribbon of cells on a villus of the small intestine. To determine if dominant mutations resulting in the gain of staining — the induction of a Dlb-1b-like allele — could also be detected, we examined Dlb-1a homozygous mice (SWR) 2 weeks after a single treatment with 250 mg/kg ethylnitrosourea. Mutations to the dominant allele should appear as brown ribbons on unstained villi. Such ribbons were observed in the treated group but not in controls. The mutant frequency was low compared to the frequency of Dlb-1a-like mutations reported at the Dlb-1-b allele in heterozygous mice.

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在Dlb-1位点诱导显性体细胞突变
在杂合小鼠的小肠(Dlb-1b/Dlba)中,Dlb-1等位基因导致染色的上皮。干细胞中显性Dlb-1b等位基因的突变或缺失会导致小肠绒毛上的细胞带不染色。为了确定是否可以检测到导致染色增加的显性突变(诱导Dlb-1a样等位基因),我们在250 mg/kg乙基亚硝基脲单次处理2周后检测了Dlb-1a纯合子小鼠(SWR)。显性等位基因的突变在未染色的绒毛上表现为棕色带。在治疗组观察到这种条带,而在对照组没有。与在杂合小鼠中报道的Dlb-1-b等位基因的dlb -1a样突变频率相比,突变频率较低。
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