• 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

对小鼠白化病基因座互补基因型的育性研究。

Fertility studies of complementing genotypes at the albino locus of the mouse.

作者信息

Lewis S E, Turchin H A, Wojtowicz T E

出版信息

J Reprod Fertil. 1978 Jul;53(2):197-202. doi: 10.1530/jrf.0.0530197.

DOI:10.1530/jrf.0.0530197
PMID:690964
Abstract

Mice doubly heterozygous for two radiation-induced lethal alleles at the albino locus (C3H and C6H) show partial complementation: they are viable but runted and sterile. In C3H/C6H females oogenesis and mating are normal, but nearly all of their fetuses, even when genotypically normal (+/C3H or +/C6H), fail to survive beyond midgestation. Abnormalities of spermatogenesis, i.e. morphological defects in head condensation and a deficiency in numbers of maturing spermatids, are histologically detectable in the testes of C3H/C6H males. Spermatozoa from the vasa deferentia of such males are predominantly nonviable, immotile, and grossly abnormal in morphology.

摘要

在白化病位点(C3H和C6H)因两个辐射诱导的致死等位基因而双杂合的小鼠表现出部分互补:它们是存活的,但发育不良且不育。在C3H/C6H雌性小鼠中,卵子发生和交配正常,但几乎所有胎儿,即使基因型正常(+/C3H或+/C6H),也无法在妊娠中期后存活。在C3H/C6H雄性小鼠的睾丸中,组织学上可检测到精子发生异常,即头部凝聚的形态学缺陷和成熟精子数量不足。来自此类雄性小鼠输精管的精子主要是无活力、不动且形态严重异常的。

相似文献

1
Fertility studies of complementing genotypes at the albino locus of the mouse.对小鼠白化病基因座互补基因型的育性研究。
J Reprod Fertil. 1978 Jul;53(2):197-202. doi: 10.1530/jrf.0.0530197.
2
The albino deletion complex and early postimplantation survival in the mouse.小鼠中的白化缺失复合体与植入后早期存活
Development. 1988 Jan;102(1):45-53. doi: 10.1242/dev.102.1.45.
3
Mice homozygous for chromosomal deletions at the albino locus region lack specific polypeptides in two-dimensional gels.在白化病基因座区域存在染色体缺失的纯合小鼠,在二维凝胶中缺乏特定的多肽。
Proc Natl Acad Sci U S A. 1984 Apr;81(7):2132-6. doi: 10.1073/pnas.81.7.2132.
4
Spermatogenesis revisited. III. The course of spermatogenesis in a male-sterile pink-eyed mutant type in the mouse.精子发生再探讨。III. 小鼠雄性不育粉眼突变型的精子发生过程。
Cell Tissue Res. 1977 May 16;180(2):173-86. doi: 10.1007/BF00231950.
5
Long-chain fatty acid triglyceride (TG) metabolism disorder impairs male fertility: a study using adipose triglyceride lipase deficient mice.长链脂肪酸三酰甘油 (TG) 代谢紊乱损害男性生育能力:脂肪甘油三酯酶缺乏小鼠的研究。
Mol Hum Reprod. 2017 Jul 1;23(7):452-460. doi: 10.1093/molehr/gax031.
6
Localization of cloned mouse chromosome 7-specific DNA to lethal albino deletions.
Somat Cell Mol Genet. 1984 May;10(3):211-5. doi: 10.1007/BF01535243.
7
Transgene insertion induced dominant male sterility and rescue of male fertility using round spermatid injection.转基因插入诱导显性雄性不育及利用圆形精子细胞注射恢复雄性育性
Biol Reprod. 2002 Mar;66(3):726-34. doi: 10.1095/biolreprod66.3.726.
8
Symplastic spermatids (sys): a recessive insertional mutation in mice causing a defect in spermatogenesis.共质体精子细胞(sys):小鼠中的一种隐性插入突变,导致精子发生缺陷。
Proc Natl Acad Sci U S A. 1990 Jul;87(13):5016-20. doi: 10.1073/pnas.87.13.5016.
9
NTP technical report on the toxicity studies of Dibutyl Phthalate (CAS No. 84-74-2) Administered in Feed to F344/N Rats and B6C3F1 Mice.美国国家毒理学计划关于邻苯二甲酸二丁酯(化学物质登记号84 - 74 - 2)经饲料给予F344/N大鼠和B6C3F1小鼠的毒性研究技术报告。
Toxic Rep Ser. 1995 Apr;30:1-G5.
10
Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies.小鼠白化病基因座区域分析:IV. 34种缺失的特征描述
Genetics. 1982 Mar;100(3):427-53. doi: 10.1093/genetics/100.3.427.

引用本文的文献

1
N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations.对小鼠7号染色体Fah-Hbb区间6至11厘摩的亚区域进行N-乙基-N-亚硝基脲诱变:已完成对4557个配子的测试以及对31个突变的缺失定位和互补分析。
Genetics. 1999 May;152(1):373-83. doi: 10.1093/genetics/152.1.373.
2
Deletion mapping of four loci defined by N-ethyl-N-nitrosourea-induced postimplantation-lethal mutations within the pid-Hbb region of mouse chromosome 7.对由N-乙基-N-亚硝基脲诱导的小鼠7号染色体pid-Hbb区域内植入后致死突变所定义的四个基因座进行缺失定位。
Genetics. 1993 Dec;135(4):1117-23. doi: 10.1093/genetics/135.4.1117.
3
Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of development.
辐射诱导的白化病(c)位点突变的分子分析,这些突变在发育的植入前阶段导致死亡。
Genetics. 1993 Dec;135(4):1107-16. doi: 10.1093/genetics/135.4.1107.
4
Genetic and physical mapping of the fitness 1 (fit1) locus within the Fes-Hbb region of mouse chromosome 7.小鼠7号染色体Fes-Hbb区域内适应性1(fit1)基因座的遗传和物理图谱。
Mamm Genome. 1995 Feb;6(2):70-5. doi: 10.1007/BF00303247.
5
Mice homozygous for chromosomal deletions at the albino locus region lack specific polypeptides in two-dimensional gels.在白化病基因座区域存在染色体缺失的纯合小鼠,在二维凝胶中缺乏特定的多肽。
Proc Natl Acad Sci U S A. 1984 Apr;81(7):2132-6. doi: 10.1073/pnas.81.7.2132.
6
Molecular mapping within the mouse albino-deletion complex.小鼠白化缺失复合体中的分子图谱分析
Proc Natl Acad Sci U S A. 1989 Nov;86(22):8862-6. doi: 10.1073/pnas.86.22.8862.
7
A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis.一种通过高效诱变对小鼠7号染色体6至11厘摩区域进行精细结构功能分析的策略。
Proc Natl Acad Sci U S A. 1990 Feb;87(3):896-900. doi: 10.1073/pnas.87.3.896.
8
Mouse chromosome 7.小鼠7号染色体。
Mamm Genome. 1991;1 Spec No:S97-111. doi: 10.1007/BF00656488.
9
Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development.对破坏肝脏特异性基因调控或中胚层发育的小鼠白化缺失进行物理分析。
Mamm Genome. 1992;2(1):51-63. doi: 10.1007/BF00570440.
10
Mouse chromosome 7.小鼠7号染色体。
Mamm Genome. 1992;3 Spec No:S104-20. doi: 10.1007/BF00648425.