Important biological variables that can influence the degree of chemical-induced aneuploidy in mammalian oocyte and zygotes

John B. Mailhes
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引用次数: 33

Abstract

The ability of certain chemicals to increase the frequency of aneuploidy in mammalian oocytes elicits concern about human health and well-being. This concernment exists because aneuploidy is the most prevalent class of human genetic disorders, and very little information exists about the etiology of aneuploidy. Although there are experimental models for studying aneuploidy in female germ cells and zygotes, these models are still being validated because insufficient information exists about the biological variables that can influence the degree of chemical-induced aneuploidy. In this regard, variables such as dose, solvent, use of gonadotrophins, mode and preovulatory time of chemical administration, time of cell harvest relative to the possibility of chemical-induced meiotic delay, criteria for cytogenetic analysis and data reporting, and an introduction to differences between cell types and sexes are presented.

Besides these variables, additional information is needed about the various molecular mechanisms associated with oocyte meiotic maturation and the genesis of aneuploidy. Also, differences between the results from selected chromosome analysis and DNA-hybridization studies are presented. Based upon the various biologic endpoints measured and the differences in cellular physiology and biochemical pathways, agreement among the results from different aneuploidy assays cannot necessarily be expected.

To gain further insight into the etiology of aneuploidy in female germ cells, information is needed about the chemical interactions between endogenous and exogenous compounds and those involved with oocyte meiotic maturation.

影响哺乳动物卵母细胞和受精卵化学诱导非整倍体程度的重要生物学变量
某些化学物质增加哺乳动物卵母细胞非整倍体频率的能力引起了人们对人类健康和福祉的关注。之所以存在这种担忧,是因为非整倍体是人类遗传疾病中最普遍的一类,而关于非整倍体病因的信息却很少。虽然有研究女性生殖细胞和受精卵非整倍体的实验模型,但这些模型仍处于验证阶段,因为关于影响化学诱导的非整倍体程度的生物学变量的信息不足。在这方面,变量,如剂量,溶剂,促性腺激素的使用,化学给药的方式和排卵前时间,细胞收获时间相对于化学诱导减数分裂延迟的可能性,细胞遗传学分析和数据报告的标准,并介绍了细胞类型和性别之间的差异。除了这些变量外,还需要了解与卵母细胞减数分裂成熟和非整倍体发生有关的各种分子机制。此外,从选择的染色体分析和dna杂交研究的结果之间的差异提出。基于测量的不同生物学终点和细胞生理学和生化途径的差异,不同非整倍体测定结果之间的一致性不一定是预期的。为了进一步了解女性生殖细胞非整倍体的病因,需要了解内源性和外源性化合物与卵母细胞减数分裂成熟相关化合物之间的化学相互作用。
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