Abstract

Although numerous attempts have been made to alter the sex ratio of the progeny of mammals, the limitations of current technologies have prevented their widespread use in farm animals. The presence or absence of a Y chromosome determines whether a mammalian embryo develops as a male or female, and non-invasive genetic reporters such as fluorescence protein markers have been intensively applied in a variety of fields of research. To develop a non-invasive and instantaneous method for advance determination of the sex of embryos, we developed a Y chromosome-linked eGFP mouse line that stably expresses green fluorescent protein under the control of the CAG promoter. The development of the CRISPR/Cas9 system has made it easy to deliver an exogenous gene to a specific locus of a genome, and linking a tracer to the Y chromosome has simplified the process of predicting the sex of embryos collected by mating a Y-Chr-eGFP transgenic male with a wild-type female. XY embryos appeared green, under a fluorescence microscope, and XX embryos did not. Y chromosome-linked genes were amplified by nested PCR to further confirm the accuracy of this method, and the simultaneous transplantation of green and non-green embryos into foster mothers indicated that 100% accuracy was achieved by this method. Thus, the Y-Chr-eGFP mouse line provides an expeditious and accurate approach for sexing pre-implantation embryos and can be efficiently used for the pre-selection of sex.

Highlights

  • A non-invasive genetic marker has been reported to allow pre-selection of the sex of progeny[7]: a D4/ XEGFP transgenic mouse line harbouring an X-linked GFP was generated by embryonic stem (ES) cell-mediated transgenesis in this study, but the incorporation of the GFP gene was random

  • These techniques include embryo karyotyping[33], fluorescence in situ hybridization (FISH) based on a sex chromosome-specific DNA probe[34], and PCR-based assays[35,36,37], but the sexing efficiencies of these techniques are closely related to the size of the embryo biopsy and may result in decreased pregnancy rates following the transfer of desmi-embryos[38,39]

  • The CRISPR/Cas[9] system has been used to produce gene-edited animals by the microinjection of Cas[9] mRNA, single guide RNA (sgRNA), and a donor template into the cytoplasm of zygotes, which greatly shortens the amount of time required for producing transgenic animals

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Summary

Introduction

A non-invasive genetic marker has been reported to allow pre-selection of the sex of progeny[7]: a D4/ XEGFP transgenic mouse line harbouring an X-linked GFP was generated by embryonic stem (ES) cell-mediated transgenesis in this study, but the incorporation of the GFP gene was random. As one type of non-invasive genetic reporter, fluorescence proteins have been applied in many fields of research, such as identifying the genotype of transgenic animals[12,13,14], tracing a specific cell lineage[15,16], and studying the expression status of genes in time and space[7,17,18]. A ubiquitously expressed sex chromosome-linked reporter gene could be used to indicate the presence of an X or Y chromosome in the mouse embryo. A Y-linked transgenic mouse line could more stably transmit a genetic marker to single-sex progeny, and the presence of a labelled marker in the Y chromosome enables visual detection of the sex of embryos and animals. The ubiquitous expression of enhanced green fluorescence protein in males can be directly linked to sex and is suitable for routine embryo sex identification in mammals

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