Scientists create sperm-producing female fish by turning off a single gene

By Christie Wilcox | June 12, 2015 8:00 am

sperm_eggAs far as natural selection is concerned, sex is just about everything. All activities a creature engages in are in service of reproduction. Not surprisingly, the nitty gritty cellular details of reproductive biology are thus of extreme interest to many scientists.

Biologically speaking, males are the members of a species that generate sperm while females produce eggs. But now, scientists from Japan have shown that a female fish can produce fully-functioning sperm—and would all the time, if it weren’t for the expression of a single gene.

Offspring from sexually reproducing species begin when two reproductive cells, called gametes, from their parents fuse. But not all gametes are the same; for reasons that still remain somewhat of a mystery, one parent donates a much larger gamete, the egg, while the other donates only essential genetic material in the form of sperm. Sperm are cheap — as they consist of little more than DNA packed in a swimming case, they are produced by males in unfathomably large numbers while females pour several thousand times more energy into producing their fewer, precious eggs. Understanding the underlying differences between egg and sperm production can help scientists learn more about the evolution of sex itself, as well as potential ways to treat medical conditions such as infertility.

A team of scientists based at the Laboratory of Molecular Genetics for Reproduction at the National Institute for Basic Biology in Okazaki, Japan, were studying the reproductive biology of a small minnow-y fish called the medaka (Oryzias latipes), a member of the ricefishes. They identified a gene which was active in the egg cells but not in the surrounding ovary tissues — foxl3 — and sought to determine its purpose by creating knockout fish lineage that lacks expression of that gene.

To their surprise, when foxl3 was supressed, the otherwise female fish started mostly producing sperm instead of eggs. But even more strangely, these female fish with no foxl3 expression began producing sperm only a week after hatching, a whole three weeks earlier than their wild male counterparts. The sperm themselves were perfectly functional — when the team used these female-made sperm to artificially inseminate eggs from wild-type female fish, they worked just fine, and most of those fertilized eggs hatched into living, healthy baby fish. The knockout males were seemingly unaffected by the loss of foxl3.

Their results, published this week in Science, suggests that, at least in the medaka, a single gene suppresses ‘maleness’ in developing reproductive cells. These data are in stark contrast to previous research in mammals, as they suggest that the ‘default’ track for gametes is to become sperm rather than eggs.

A Female medaka lacking foxl3 genes, looking very much like a normal female medaka.  But her ovaries (lower images) tell a different story; lots of sperm produced alongside a handful of eggs. Image provided by the National Institute for Basic Biology

A Female medaka lacking foxl3 genes, looking very much like a normal female medaka — but her ovaries (lower images) tell a different story. In them are lots of sperm alongside a handful of eggs. Image provided by the National Institute for Basic Biology

 

However, this isn’t the first time a foxl gene implicated in maintaining femaleness. Back in 2009, scientists found that female mice will produce testes instead of ovaries, even as adults, if the gene foxl2 is knocked out. But in that case, the entire reproductive organ changed from female to male. These fish are able to develop healthy male gametes inside a very female ovary.

“In spite of the environment surrounding the germ cells being female, the fact that functional sperm has been made surprised me greatly. That this sexual switch present in the germ cells is independent of the body’s sex is an entirely new finding” first author Toshiya Nishimura told Reuters.

Future research may investigate similar genes in mammals to see if we, too, have a sperm-suppressing gene that ensures our egg cells stay on track. For now, though, the team is continuing their study of foxl3 in fish to discover how exactly it works. They’re interested in determining what regulates its expression as well as what the gene product actually does to prevent gametes from becoming sperm.

 

Citation: Toshiya NishimuraTetsuya SatoYasuhiro YamamotoIkuko WatakabeYasuyuki OhkawaMikita SuyamaSatoru Kobayashiand Minoru Tanaka (2015). foxl3 is a germ cell-intrinsic factor involved in sperm-egg fate decision in medaka. Science DOI:10.1126/science.aaa2657

CATEGORIZED UNDER: More Science, select, Top Posts
ADVERTISEMENT
  • OWilson

    A possible therapy for the LGBT community.
    A new race of Amazons. Males finally eliminated.
    And a political debate whether Obamacare will provide it, or indeed whether male taxpayers should be required to fund it.
    Sometimes science gets ahead of sociology :)

    • Solgirl

      Um, Amazons were noted warriors so I wouldn’t look for wars to go away too soon,

  • paulflag

    Great! Another reason for Women not need Men?? TIC 😉

  • Liz Hall

    So where do the altered females actually make the sperm? In their ovaries?

    • Antoinette Reyes

      By the sound of the article, yes.

    • OWilson

      Sounds like in-utero cloning.

      Could be a big deal for women who would like to raise a child without the hassle of finding and keeping a husband.

      I’m being serious here.

  • Sandi

    this is a tragedy…women already don’t have much use for us men…

  • Anne Kabugi

    Good because bleeding will be only for a woman.

  • robert tjin

    If someone says it’s cloning, that’s big wrong. And, why don’t they try it to humans? Sounds fair enough.

NEW ON DISCOVER
OPEN
CITIZEN SCIENCE
ADVERTISEMENT

Science Sushi

Real Science. Served Raw.

About Christie Wilcox

Dr. Christie Wilcox is a science writer and postdoctoral scholar at the University of Hawaii. She freelances for major media outlets including The New York Times and Popular Science. Her debut book, Venomous, releases August 2016 (Scientific American/FSG Books). To learn more about her life and work, check out her webpage or follow her on Twitter, Google+, or Facebook.

ADVERTISEMENT

See More

ADVERTISEMENT

@NerdyChristie on Twitter

Discover's Newsletter

Sign up to get the latest science news delivered weekly right to your inbox!

Collapse bottom bar
+