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种内回交卷尾小鼠的单倍型分析证实了ct基因定位于4号染色体。

Haplotype analysis of intra-specific backcross curly-tail mice confirms the localization of ct to chromosome 4.

作者信息

Beier D R, Dushkin H, Telle T

机构信息

Genetics Division, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Mamm Genome. 1995 Apr;6(4):269-72. doi: 10.1007/BF00352414.

DOI:10.1007/BF00352414
PMID:7613032
Abstract

We have determined the order of a number of SSR and SSC polymorphic markers that map to distal mouse Chromosome (Chr) 4 and have used analysis of these markers in backcrosses designed to test the localization of the curly-tail (ct) mutation. We have confirmed that ct maps to this region, close to the locus D4Mit69. Our results also support the hypothesis that ct is a semidominant, rather than a recessive, mutation, since we have identified abnormal-tailed mice that are likely to be heterozygous at the ct locus. Finally, we examined Pax7 as a candidate gene for the ct mutation and found no evidence of protein sequence differences in ct compared with wild-type mice.

摘要

我们已经确定了多个映射到小鼠4号染色体远端的简单序列重复(SSR)和简单序列簇(SSC)多态性标记的顺序,并在用于测试卷尾(ct)突变定位的回交实验中对这些标记进行了分析。我们已经证实ct定位于该区域,靠近D4Mit69位点。我们的结果还支持这样的假设,即ct是一种半显性而非隐性突变,因为我们已经鉴定出在ct位点可能为杂合子的异常尾巴小鼠。最后,我们将Pax7作为ct突变的候选基因进行了检测,未发现与野生型小鼠相比ct在蛋白质序列上存在差异的证据。

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1
Haplotype analysis of intra-specific backcross curly-tail mice confirms the localization of ct to chromosome 4.种内回交卷尾小鼠的单倍型分析证实了ct基因定位于4号染色体。
Mamm Genome. 1995 Apr;6(4):269-72. doi: 10.1007/BF00352414.
2
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Curly tail: a 50-year history of the mouse spina bifida model.卷尾:小鼠脊柱裂模型的50年历史。

本文引用的文献

1
Intrinsic and extrinsic factors in the mechanism of neurulation: effect of curvature of the body axis on closure of the posterior neuropore.神经管形成机制中的内在和外在因素:身体轴曲率对后神经孔闭合的影响。
Development. 1993 Mar;117(3):1163-72. doi: 10.1242/dev.117.3.1163.
2
A Macintosh program for storage and analysis of experimental genetic mapping data.一个用于存储和分析实验性基因图谱数据的麦金塔程序。
Mamm Genome. 1993;4(6):303-13. doi: 10.1007/BF00357089.
3
Single-strand conformation polymorphism (SSCP) analysis as a tool for genetic mapping.
Anat Embryol (Berl). 2001 Apr;203(4):225-37. doi: 10.1007/s004290100169.
4
The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse chromosome 4.
Mamm Genome. 1996 Nov;7(11):864-5. doi: 10.1007/s003359900255.
5
Relationship between altered axial curvature and neural tube closure in normal and mutant (curly tail) mouse embryos.正常和突变(卷尾)小鼠胚胎中轴曲率改变与神经管闭合之间的关系。
Anat Embryol (Berl). 1996 Feb;193(2):123-30. doi: 10.1007/BF00214703.
单链构象多态性(SSCP)分析作为一种基因定位工具。
Mamm Genome. 1993 Nov;4(11):627-31. doi: 10.1007/BF00360898.
4
Interaction between splotch (Sp) and curly tail (ct) mouse mutants in the embryonic development of neural tube defects.斑点(Sp)和卷尾(ct)小鼠突变体在神经管缺陷胚胎发育中的相互作用。
Development. 1993 Sep;119(1):113-21. doi: 10.1242/dev.119.1.113.
5
Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice.神经管缺陷的多因素遗传:ct突变小鼠中主要基因的定位及修饰基因的识别
Nat Genet. 1994 Apr;6(4):357-62. doi: 10.1038/ng0494-357.
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.
7
undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1.波状(undulated)是一种影响小鼠骨骼发育的突变,它在Pax 1的配对盒中有一个点突变。
Cell. 1988 Nov 4;55(3):531-5. doi: 10.1016/0092-8674(88)90039-6.
8
Does lumbosacral spina bifida arise by failure of neural folding or by defective canalisation?腰骶部脊柱裂是由于神经折叠失败还是神经管形成缺陷引起的?
J Med Genet. 1989 Mar;26(3):160-6. doi: 10.1136/jmg.26.3.160.
9
The murine paired box gene, Pax7, is expressed specifically during the development of the nervous and muscular system.
Mech Dev. 1990 Dec;33(1):27-37. doi: 10.1016/0925-4773(90)90132-6.
10
Pax: a murine multigene family of paired box-containing genes.Pax:一个包含成对盒基因的小鼠多基因家族。
Genomics. 1991 Oct;11(2):424-34. doi: 10.1016/0888-7543(91)90151-4.