• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

四只体内重组小鼠的分子特征分析。

Molecular characterization of four intra-t mouse recombinants.

作者信息

Mizuno K, Vincek V, Figueroa F, Klein J

机构信息

Max-Planck-Institut für Biologie, Abteilung Immungenetik, Tübingen, Federal Republic of Germany.

出版信息

Immunogenetics. 1989;30(2):112-8. doi: 10.1007/BF02421539.

DOI:10.1007/BF02421539
PMID:2759663
Abstract

Recombination in the proximal region of mouse chromosome 17 is greatly reduced in heterozygotes carrying the wild-type and the t complex-type chromosomes. The reason for this is the presence of two non-overlapping inversions in the t complex. Rare crossing-over does, however, occur within the t complex of the t/+ heterozygotes. Here we characterize four such exceptional intra-t recombinants, tTu1 through tTu4. To map the positions of the genetic exchange in these four recombinants, we analyzed them with DNA probes specific for 16 loci distributed over the t complex. The analysis revealed that in three of the four recombinants, an equal crossing-over occurred in the short region between the two inversions, producing chromosomes carrying either the proximal inversion only (tTu1 and tTu4) or the distal inversion only (tTu2). In the fourth recombinant (tTu3), unequal crossing-over occurred within the proximal inversion between loci D17Leh119 and D17Leh66, producing a chromosome in which the region containing loci Tcp-1, T, and D17Tu5 has been duplicated. The duplication of the Brachyury locus leads to the suppression of the tail-shortening effect normally produced by the interaction of the dominant (T) and recessive (tct) alleles at this locus so that the T/tTu3 mice have normal tails.

摘要

在携带野生型和t复合体型染色体的杂合子中,小鼠17号染色体近端区域的重组大大减少。原因是t复合体中存在两个不重叠的倒位。然而,在t/+杂合子的t复合体内确实会发生罕见的交叉互换。在此,我们鉴定了四个这样的特殊t复合体内重组体,即tTu1至tTu4。为了定位这四个重组体中基因交换的位置,我们用分布在t复合体上的16个位点的特异性DNA探针分析了它们。分析表明,在四个重组体中的三个中,在两个倒位之间的短区域发生了均等交叉互换,产生了仅携带近端倒位(tTu1和tTu4)或仅携带远端倒位(tTu2)的染色体。在第四个重组体(tTu3)中,在近端倒位内的D17Leh119和D17Leh66位点之间发生了不等交叉互换,产生了一条染色体,其中包含Tcp-1、T和D17Tu5位点的区域被重复。短尾基因座的重复导致了通常由该基因座上显性(T)和隐性(tct)等位基因相互作用产生的尾巴缩短效应受到抑制,因此T/tTu3小鼠具有正常的尾巴。

相似文献

1
Molecular characterization of four intra-t mouse recombinants.四只体内重组小鼠的分子特征分析。
Immunogenetics. 1989;30(2):112-8. doi: 10.1007/BF02421539.
2
Evidence for unequal crossing over within the mouse T/t complex.小鼠T/t复合体中不等交换的证据。
Proc Natl Acad Sci U S A. 1980 Oct;77(10):6077-80. doi: 10.1073/pnas.77.10.6077.
3
Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes.小鼠17号染色体的进化及与t单倍型相关的倒位起源
Proc Natl Acad Sci U S A. 1989 May;86(9):3261-5. doi: 10.1073/pnas.86.9.3261.
4
Limits of the distal inversion in the t complex of the house mouse: evidence from linkage disequilibria.家鼠t复合体中远端倒位的限度:来自连锁不平衡的证据。
Mamm Genome. 1991;1(4):242-8. doi: 10.1007/BF00352331.
5
Nonhomologous pairing in mice heterozygous for a t haplotype can produce recombinant chromosomes with duplications and deletions.对于携带t单倍型的杂合小鼠,非同源配对可产生具有重复和缺失的重组染色体。
Genetics. 1986 Jul;113(3):723-34. doi: 10.1093/genetics/113.3.723.
6
Extent of the mouse t complex and its inversions shown by in situ hybridization.通过原位杂交显示的小鼠t复合体及其倒位的范围。
Immunogenetics. 1988;27(5):375-82. doi: 10.1007/BF00395134.
7
Genetic evidence for two t complex tail interaction (tct) loci in t haplotypes.t单倍型中两个t复合尾部相互作用(tct)位点的遗传证据。
Genetics. 1989 Aug;122(4):895-903. doi: 10.1093/genetics/122.4.895.
8
Gene mapping within the T/t complex of the mouse. I. t-Lethal genes are nonallelic.小鼠T/t复合体内的基因定位。I. t致死基因是非等位基因。
Cell. 1982 Mar;28(3):463-70. doi: 10.1016/0092-8674(82)90200-8.
9
Genetic exchange across a paracentric inversion of the mouse t complex.小鼠t复合体臂内倒位的基因交换
Genetics. 1991 Aug;128(4):799-812. doi: 10.1093/genetics/128.4.799.
10
Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes.使用新的分子探针和部分t单倍型对小鼠t复合体近端区域进行遗传和分子分析。
Genetics. 1990 Dec;126(4):1103-14. doi: 10.1093/genetics/126.4.1103.

引用本文的文献

1
The D17Tu5 locus in the t complex: implications for the origin of t haplotypes and inbred strains.t 复合体中的 D17Tu5 位点:对 t 单倍型和近交系起源的影响。
Immunogenetics. 1989;30(2):105-11. doi: 10.1007/BF02421538.
2
Low diversity of t haplotypes in the eastern form of the house mouse, Mus musculus L.小家鼠(Mus musculus L.)东部形态中t单倍型的低多样性
Genetics. 1991 Jan;127(1):161-8. doi: 10.1093/genetics/127.1.161.
3
Maps of mouse chromosome 17: first report. Committee for Mouse Chromosome 17.小鼠第17号染色体图谱:首次报告。小鼠第17号染色体委员会。

本文引用的文献

1
Genetic Change in Mutations at the T/t-Locus in the Mouse.在小鼠 T/t 基因座的突变中的遗传变化。
Genetics. 1976 Jun;83(2):361-72. doi: 10.1093/genetics/83.2.361.
2
INVESTIGATIONS OF THE NATURE OF T-ALLELES IN THE MOUSE. III. SHORT TESTS OF SOME FURTHER MUTANT ALLELES.小鼠T等位基因性质的研究。III. 一些其他突变等位基因的简短测试。
Heredity (Edinb). 1964 May;19:327-30. doi: 10.1038/hdy.1964.35.
3
INVESTIGATIONS OF THE NATURE OF T-ALLELES IN THE MOUSE. II. GENETIC ANALYSIS OF AN UNUSUAL MUTANT ALLELE AND ITS DERIVATIVES.小鼠T等位基因性质的研究。II. 一个异常突变等位基因及其衍生物的遗传分析。
Mamm Genome. 1991;1(1):5-29.
Heredity (Edinb). 1964 May;19:313-25. doi: 10.1038/hdy.1964.34.
4
INVESTIGATIONS OF THE NATURE OF T-ALLELES IN THE MOUSE. I. GENETIC ANALYSIS OF A SERIES OF MUTANTS DERIVED FROM A LETHAL ALLELE.小鼠T等位基因性质的研究。I. 源自一个致死等位基因的一系列突变体的遗传分析。
Heredity (Edinb). 1964 May;19:301-12. doi: 10.1038/hdy.1964.33.
5
Evidence for two regions in the mouse t complex controlling transmission ratios.小鼠t复合体中控制传递比率的两个区域的证据。
Genet Res. 1981 Dec;38(3):315-25. doi: 10.1017/s0016672300020632.
6
Gene mapping within the T/t complex of the mouse. II. Anomalous position of the H-2 complex in t haplotypes.小鼠T/t复合体中的基因定位。II. H-2复合体在t单倍型中的异常位置。
Cell. 1982 Mar;28(3):471-6. doi: 10.1016/0092-8674(82)90201-x.
7
Transmission ratio distortion in mouse t-haplotypes is due to multiple distorter genes acting on a responder locus.小鼠t单倍型中的传递比率畸变是由于多个畸变基因作用于一个反应位点所致。
Cell. 1984 Jun;37(2):621-8. doi: 10.1016/0092-8674(84)90393-3.
8
Characterization of a recombinant mouse T haplotype that expresses a dominant lethal maternal effect.表达显性致死母本效应的重组小鼠T单倍型的特征分析。
Genetics. 1984 Dec;108(4):1013-20. doi: 10.1093/genetics/108.4.1013.
9
An alpha globin pseudogene is located within the mouse t complex.一个α珠蛋白假基因位于小鼠t复合体内部。
Immunogenetics. 1984;19(2):125-30. doi: 10.1007/BF00387855.
10
Dispersion of alpha-like globin genes of the mouse to three different chromosomes.小鼠α样珠蛋白基因分散至三条不同染色体上。
Nature. 1981;293(5829):196-200. doi: 10.1038/293196a0.