Beechey C V, Searle A G
M.R.C. Radiobiology Unit, Chilton, Didcot, Oxon, UK.
Cytogenet Cell Genet. 1991;56(1):2-8. doi: 10.1159/000133034.
A new murine tester stock for primary nondisjunction incorporates three genetically marked Robertsonian translocations with tribrachial homology (TBH): Rb(6.15)1Ald, Rb(4.6)2Bnr, and Rb(4.15)4Rma. The resultant tricentromeric meiotic configuration leads to 100% aneuploid gametes, but the TBH stock can be maintained by intercrossing, through the complementation of nullisomic and disomic gametes. The only neonatal survivors from tescrosses to wild type come from complementation of aneuploid gametes and genetic tests allow wild type gains or losses of Chromosomes 4, 6, and 15 to be distinguished. Alternatively, cytogenetic examination allows products of wild type chromosome gain, with one metacentric, to be separated from chromosome loss with two metacentrics. A pilot study, with 0-2 Gy X-irradiation of oocytes at diakinesis, revealed twelve examples of chromosome loss in wild type gametes but none of chromosome gain and thus provided no evidence for the induction of nondisjunction.
一种用于原发性不分离的新型小鼠测试品系包含三个具有三臂同源性(TBH)的基因标记罗伯逊易位:Rb(6.15)1Ald、Rb(4.6)2Bnr和Rb(4.15)4Rma。由此产生的三着丝粒减数分裂构型会导致100%的非整倍体配子,但通过零体和二体配子的互补,可通过杂交维持TBH品系。与野生型回交产生的仅有的新生存活者来自非整倍体配子的互补,并且基因检测能够区分4号、6号和15号染色体的野生型增加或缺失。另外,细胞遗传学检查能够将具有一条中着丝粒染色体的野生型染色体增加产物与具有两条中着丝粒染色体的染色体缺失产物区分开来。一项对处于终变期的卵母细胞进行0 - 2 Gy X射线照射的初步研究,在野生型配子中发现了12个染色体缺失的例子,但没有染色体增加的情况,因此没有提供诱导不分离的证据。