Laboratory of Genetics, University of Wisconsin-Madison.
Laboratory of Genetics, University of Wisconsin-Madison;
J Vis Exp. 2021 Dec 21(178). doi: 10.3791/63177.
Early development depends on a pool of maternal factors incorporated into the mature oocyte during oogenesis that perform all cellular functions necessary for development until zygotic genome activation. Typically, genetic targeting of these maternal factors requires an additional generation to identify maternal-effect phenotypes, hindering the ability to determine the role of maternally-expressed genes during development. The discovery of the biallelic editing capabilities of CRISPR-Cas9 has allowed screening of embryonic phenotypes in somatic tissues of injected embryos or "crispants," augmenting the understanding of the role zygotically-expressed genes play in developmental programs. This article describes a protocol that is an extension of the crispant method. In this method, the biallelic editing of germ cells allows for the isolation of a maternal-effect phenotype in a single generation, or "maternal crispants." Multiplexing guide RNAs to a single target promotes the efficient production of maternal crispants, while sequence analysis of maternal crispant haploids provides a simple method to corroborate genetic lesions that produce a maternal-effect phenotype. The use of maternal crispants supports the rapid identification of essential maternally-expressed genes, thus facilitating the understanding of early development.
早期发育依赖于在卵子发生过程中整合到成熟卵母细胞中的母体因子池,这些因子执行发育所需的所有细胞功能,直到合子基因组激活。通常,这些母体因子的遗传靶向需要额外的一代来鉴定母体效应表型,这阻碍了确定母源表达基因在发育过程中的作用的能力。CRISPR-Cas9 的双等位基因编辑能力的发现允许在注射胚胎的体组织或“crispants”中筛选胚胎表型,从而增强了对合子表达基因在发育程序中所起作用的理解。本文描述了一种扩展 crispant 方法的方案。在该方法中,生殖细胞的双等位基因编辑允许在单个世代中分离母体效应表型,或“母体 crispants”。将多个向导 RNA 靶向单个靶标可促进母体 crispants 的高效产生,而母体 crispants 单倍体的序列分析提供了一种简单的方法来证实产生母体效应表型的遗传损伤。母体 crispants 的使用支持快速鉴定必需的母源表达基因,从而促进对早期发育的理解。