{"id":3226,"date":"2021-12-08T18:27:25","date_gmt":"2021-12-08T18:27:25","guid":{"rendered":"http:\/\/blogs.kent.ac.uk\/biosciences\/?p=3226"},"modified":"2021-12-08T18:27:25","modified_gmt":"2021-12-08T18:27:25","slug":"researchers-use-gene-editing-to-create-single-sex-mice-litters","status":"publish","type":"post","link":"https:\/\/blogs.kent.ac.uk\/biosciences\/2021\/12\/08\/researchers-use-gene-editing-to-create-single-sex-mice-litters\/","title":{"rendered":"Researchers use gene-editing to create single sex mice litters"},"content":{"rendered":"

Researchers from Kent\u2019s\u00a0School of Biosciences<\/a>\u00a0and\u00a0the\u00a0Francis Crick Institute<\/a>\u00a0have used gene editing technology to create female-only and male-only mice litters with 100% efficiency.<\/p>\n

This proof of principle study, published in\u00a0Nature Communications<\/em>, demonstrates how the technology could be used to improve animal welfare in scientific research and perhaps also agriculture.<\/p>\n

In scientific research and also farming, there is often a need for either male or female animals. For example, laboratory research into male or female reproduction requires only animals of the sex being studied. And in farming, only female animals are required for egg production and in dairy herds. This means it is common practice for animals of the unrequired sex to be culled after birth.<\/p>\n

The researchers\u2019 new method uses a two-part genetic system to inactivate embryos shortly after fertilisation, allowing only the desired sex to develop. Such a genetically-based method to control the sex of offspring could drastically reduce culling in both industries.<\/p>\n

The embryo selection is based on the fact that there are two elements of CRISPR-Cas9 \u2013 the Cas9 enzyme that cuts the DNA, allowing scientists to alter specific regions, and the guide RNA which carries the Cas9 to the right location on the genome. The team placed one element of the system on the father\u2019s X or Y chromosome, meaning that it will only be inherited by female or male embryos respectively. The other element is contributed by the mother, and is inherited by all embryos.<\/p>\n

They targeted the\u00a0Top1<\/em>\u00a0gene, which is essential to DNA replication and repair. When an embryo formed from a sperm and egg, each containing one half of CRISPR-Cas9, the gene-editing was triggered in the embryo and it was not able to develop beyond a very early stage of around 16 to 32 cells.<\/p>\n

Using this method, the researchers were able to control, with 100% effect, the sex of a litter. To produce a male-only litter, the researchers edited the father\u2019s X chromosome, meaning only females inherited the deleterious mutation, and for a female-only litter, they edited the Y chromosome.<\/p>\n

Surprisingly, the method did not lead to a 50% decrease in the number of offspring produced, rather the litter sizes were between 61% \u2013 72% of the control litters. The researchers suggest this is because animals such as mice produce more eggs than required during each ovarian cycle, allowing for a proportion of them to be lost during early development without reducing litter size. This means that in situations where one sex is needed, fewer breeding animals will be required in order to produce the same number of the desired sex of offspring.<\/p>\n

As the\u00a0Top1<\/em>\u00a0gene is well conserved across mammals, these results may also be applicable to other animals.<\/p>\n

Charlotte Douglas, first author and former PhD student and postdoctoral scientist at the Crick, says: \u201cThis method works as we split the genome editing process in half, between a male and female, and it is only when the two halves meet in an embryo through breeding, that it is activated. Embryos with both halves cannot develop beyond very early cell stages.<\/p>\n

\u201cWe\u2019ve also shown this process works successfully in different combinations \u2013 introducing either the Cas9 or the guide RNA elements on to the mother\u2019s or father\u2019s chromosomes.\u201d<\/p>\n

As the offspring which survive only contain half of the CRISPR-Cas9 elements within their genome, this acts as a control preventing the sex-selection being passed down to further generations, unless they are selectively bred with an individual of the opposite sex containing the other half. This is different to genetic engineering through \u2018gene-drive\u2019 methods, which seek to spread a genetic mutation widely amongst a population.<\/p>\n

There are also no harmful effects of the gene edit in the surviving offspring.<\/p>\n

James Turner, author and group leader of the Sex Chromosome Biology Laboratory at the Crick says: \u2018This work could have immediate and valuable impact in scientific laboratories, as we\u2019ve shown how it is safe and effective in mice, a common mammal used in medical and scientific research. While a lot of research needs both sexes, there are areas of study where only one is needed. For example, when studying the reproductive system, sex-specific diseases, or certain hormones.<\/p>\n

Peter Ellis, author and senior lecturer in molecular genetics and reproduction at Kent, says: \u2018The implications of this work are potentially far-reaching when it comes to improving animal welfare, but should be considered at ethical and regulatory levels.<\/p>\n

\u2018In particular, before any potential use in agriculture, there would need to be extensive public conversation and debate, as well as changes to legislation. On the scientific side, there is also much work to be done over a number of years. Further research is needed, first to develop the particular gene editing toolkits for different species, and then to check they are safe and effective.\u2019<\/p>\n

The paper, \u2018CRISPR-Cas9 effectors facilitate generation of single-sex litters and sex-specific phenotypes<\/em>\u2018, is published in\u00a0Nature Communications.<\/p>\n

URL:\u00a0https:\/\/www.nature.com\/articles\/s41467-021-27227-2<\/p>\n

DOI: 10.1038\/s41467-021-27227-2.<\/p>\n