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Genes Dev. 1993 Apr;7(4):621-32. doi: 10.1101/gad.7.4.621.
2
High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation.由DNA重复介导的高频基因回复:小鼠粉红眼不稳定突变
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3
Melanocyte culture lines from Tyr-SV40E transgenic mice: models for the molecular genetic evolution of malignant melanoma.来自酪氨酸 - 猿猴病毒40大T抗原转基因小鼠的黑素细胞培养系:恶性黑色素瘤分子遗传进化的模型
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A gain-of-function mutation in Drosophila MAP kinase activates multiple receptor tyrosine kinase signaling pathways.
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Allelic loss in ovarian cancer.卵巢癌中的等位基因缺失。
Int J Cancer. 1993 Jun 19;54(4):546-51. doi: 10.1002/ijc.2910540405.
6
A genetic map of the mouse with 4,006 simple sequence length polymorphisms.一张具有4006个简单序列长度多态性的小鼠遗传图谱。
Nat Genet. 1994 Jun;7(2 Spec No):220-45. doi: 10.1038/ng0694supp-220.
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SARs do not impair position-dependent expression of a kit/lacZ transgene.
Biochem Biophys Res Commun. 1995 Jun 26;211(3):735-41. doi: 10.1006/bbrc.1995.1874.
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Effect of the Steel gene product on melanogenesis in avian neural crest cell cultures.Steel基因产物对禽类神经嵴细胞培养中黑色素生成的影响。
Differentiation. 1994 Dec;58(2):133-9. doi: 10.1046/j.1432-0436.1995.5820133.x.
9
W/kit gene required for interstitial cells of Cajal and for intestinal pacemaker activity.W/kit基因是Cajal间质细胞和肠道起搏活动所必需的。
Nature. 1995 Jan 26;373(6512):347-9. doi: 10.1038/373347a0.
10
Instability at the W/c-kit locus in mice: analysis of melanocyte cell lines derived from reversion spots.
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小鼠有丝分裂重组介导的W/Kit基因座表型回复突变

Phenotypic reversions at the W/Kit locus mediated by mitotic recombination in mice.

作者信息

De Sepulveda P, Guenet J L, Panthier J J

机构信息

URA-INRA de Génétique Moléculaire, Ecole Nationale Vétérinaire d'Alfort, France.

出版信息

Mol Cell Biol. 1995 Nov;15(11):5898-905. doi: 10.1128/MCB.15.11.5898.

DOI:10.1128/MCB.15.11.5898
PMID:7565742
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC230841/
Abstract

The mouse W locus encodes Kit, the receptor tyrosine kinase for stem cell factor (SCF). Kit is required for several developmental processes, including the proliferation and survival of melanoblasts. Because of the nearly complete failure of Wrio/+ melanoblasts to colonize the skin, the costs of Wrio/+ mice are characterized by a majority of white hairs interspersed among pigmented hairs, giving a roan effect. However, 3.6% of Wrio/+ mice exhibit phenotypic reversions, i.e., spots of wild-type color on their coats with an otherwise mutant phenotype. Melanocyte cell lines were derived from each of six independent reversion spots on the skin of (C57BL/6 x DBA/2)F1 Wrio/+ mice. All six melanocyte cell lines exhibited the general characteristics common to normal, nonimmortal mouse melanocytes. Of these, three revertant cell lines had lost the dominant-negative Wrio allele following mitotic recombination between the centromere and the W locus. One of the cell lines remained Wrio/+ but showed (i) stimulation in response to SCF and (ii) increased Kit expression, suggesting that the Wrio mutation can be rescued by increased endogenous expression of the c-kit proto-oncogene. Finally, two cell lines showed no detectable genetic change at the W/Kit locus and failed to respond to SCF stimulation in vitro. These results demonstrate that mitotic recombination can create large patches of wild-type hair on the coats of Wrio/+ mutant mice. This shows that mitotic recombination occurs spontaneously in normal healthy tissue in vivo. Moreover, these experiments confirm that other mechanisms, not associated with loss of heterozygosity, may account for the coat color reversion phenotype.

摘要

小鼠的W基因座编码Kit,它是干细胞因子(SCF)的受体酪氨酸激酶。Kit参与多个发育过程,包括黑素母细胞的增殖和存活。由于Wrio/+黑素母细胞几乎完全无法在皮肤中定植,Wrio/+小鼠的毛色特征是大部分白色毛发夹杂在有色毛发中,呈现出花斑效果。然而,3.6%的Wrio/+小鼠表现出表型逆转,即其被毛上出现野生型颜色的斑点,而其他部分表现为突变表型。黑素细胞系来源于(C57BL/6×DBA/2)F1 Wrio/+小鼠皮肤的六个独立逆转斑点。所有六个黑素细胞系都表现出正常的、未永生化的小鼠黑素细胞共有的一般特征。其中,三个回复细胞系在着丝粒和W基因座之间发生有丝分裂重组后,丢失了显性负性Wrio等位基因。其中一个细胞系仍为Wrio/+,但表现出(i)对SCF有反应,(ii)Kit表达增加,这表明Wrio突变可通过c-kit原癌基因内源性表达增加而得到挽救。最后,两个细胞系在W/Kit基因座未检测到遗传变化,且在体外对SCF刺激无反应。这些结果表明,有丝分裂重组可在Wrio/+突变小鼠的被毛上产生大片野生型毛发。这表明有丝分裂重组在体内正常健康组织中自发发生。此外,这些实验证实,其他与杂合性丧失无关的机制可能导致毛色逆转表型。