Maternal Meiotic Drive of Mouse Chromosome 11

描述（由申请人提供）：孟德尔平等传递定律 每个个体携带的两种不同形式的基因几乎 普遍的。事实上，每种基因的两种形式都被传递到 在几乎所有情况下，一个人的后代的一半表明， 很少有减数分裂的“公平性”受到损害的情况。我们有 发现了一个在雌性小鼠（称为母体）中的“不公平减数分裂”的例子。 减数分裂驱动），导致基因的优先传递， 导致下一代早期胚胎死亡。我们建议 这一过程的发生机制包括形成一个额外的“蛋 携带胚胎致死基因的染色体上的“附着位点”。这 额外的位点使得携带该基因的染色体 致命的基因将被传递到鸡蛋（并且，相应地，只有一半的基因被传递到鸡蛋）。 携带另一种形式基因的染色体很可能会 传递到鸡蛋）。我们计划在 分子水平，确定它是如何创建的，以及哪些基因参与了它的 创作控制这些站点的活动的能力可以允许人们 操纵某些特征遗传的频率。此外，本发明还提供了一种方法， 这个女性“不公平减数分裂”的例子有一个独特的组成部分， 卵细胞中“不公平减数分裂”的发生是由基因或基因产物引起的 由精子提供。我们建议鉴定这个父系基因， 它是如何影响卵子中染色体的分离的。

DESCRIPTION (provided by applicant): Mendel's law of equal transmission of the two alternative forms of a gene that are carried by each individual is nearly universal. The fact that the two forms of each gene are each transmitted to one-half of an individual's offspring in almost all cases indicates that there are few instances in which the "fairness" of meiosis is compromised. We have uncovered an example of "unfair meiosis" in female mice (called maternal meiotic drive) that results in the, preferential transmission of a gene that causes early embryo lethality in the following generation. We propose that the mechanism by which this occurs involves the formation of an additional "egg attachment site" on the chromosome that carries the embryonic lethal gene. This additional site makes it twice as likely that the chromosome carrying the lethal gene will be transmitted to the egg (and, correspondingly only half as likely that the chromosome carrying the other form of the gene will be transmitted to the egg). We plan to identify this attachment site, at the molecular level, determine how it is created and what genes are involved in its creation. The ability to control the activity of such sites may allow one to manipulate the frequency with which some traits are inherited. In addition, this example of "unfair meiosis" in females has a unique component because the onset of "unfair meiosis" in the egg is brought about by a gene or gene product provided by the sperm. We propose to identify this paternal gene and determine how it is able to influence the segregation of chromosomes in the egg.