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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome.
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Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome.

机译:小鼠的非分离率和异常胚胎发育在携带(7,18)罗伯逊易位染色体的杂合子之间交叉。

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摘要

Mice bearing Robertsonian translocation chromosomes frequently produce aneuploid gametes. They are therefore excellent tools for studying nondisjunction in mammals. Genotypic analysis of embryos from a mouse cross between two different strains of mice carrying a (7,18) Robertsonian chromosome enabled us to measure the rate of nondisjunction for chromosomes 7 and 18. Embryos (429) were harvested from 76 litters of mice and the parental origin of each chromosome 7 and 18 determined. Genotyping these embryos has allowed us to conclude the following: (1) there were 96 embryos in which at least one nondisjunction event had taken place; (2) the rate of maternal nondisjunction was greater than paternal nondisjunction for teh chromosomes sampled in these mice; (3) a bias against chromosome 7 and 18 nullisomic gametes was observed, reflected in a smaller than expected number of uniparental disomic embryos; (4) nondisjunction events did not seem to occur at random throughout the 76 mouse litters, but were clustered into fewer than would be expected cy chance; and (5) a deficiency of paternal chromosome 18 uniparental disomic embryos was observed along with a higher than normal rate of developmental retardation at 8.5 days post coitum, raising the possibility that this chromosome has at least one imprinted gene.
机译:携带罗伯逊易位染色体的小鼠经常产生非整倍体配子。因此,它们是研究哺乳动物非分离的极好工具。对携带(7,18)罗伯逊染色体的两种不同品系的小鼠杂交的胚胎进行基因型分析,使我们能够测量7号和18号染色体的非分离率。从76窝小鼠中收获了胚胎(429)。每个染色体的亲本起源分别由7和18确定。对这些胚胎进行基因分型可以使我们得出以下结论:(1)有96个胚胎中至少发生了一个非分离事件; (2)在这些小鼠中采集的染色体的母本非分离率大于母本非分离率; (3)观察到对7号染色体和18个无效染色体配子的偏见,反映在单亲二体组胚胎的数量少于预期的情况下; (4)在76个小鼠垫料中,非分离事件似乎并不是随机发生的,而是聚集在比预期的cy机会少的位置。 (5)观察到父亲染色体第18号单亲二体性胚胎缺乏,以及在宫突后8.5天发育迟缓率高于正常水平,这增加了该染色体至少有一个印记基因的可能性。

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