Showing posts with label genes. Show all posts
Showing posts with label genes. Show all posts

Thursday, October 16, 2014

Michael White - How the Sexes Evolved (via Pacific Standard)

Each Friday, Pacific Standard has been looking at how and why the social becomes biological. This week Michale White flipped the question: How does biology become social? One of the best ways to see how biology drives social behavior is to look at one of the oldest social relationships in the living world: sex.

How the Sexes Evolved

• August 15, 2014 

sex-gene
(Photo: Crystal Eye Studio/Shutterstock)
The distinction between males and females is one of the oldest facts of biology—but how did it come to affect our social identity?
Every Friday this month we’re taking a look at the relationship between the social and the biological—specifically, how and why the former becomes the latter. Check back next week for another installment.

One way to understand how and why the social becomes biological is to flip the question: How does biology become social? One of the best ways to see how biology drives social behavior is to look at one of the oldest social relationships in the living world: sex.

Sex and its central role is biology is the main reason why men and women are different, but it’s hard to tease apart biology from culture. Anatomical differences are obviously biological, while a quick survey of various human societies is enough to see that many differences between men and women are cultural and liable to change. The distinction between males and females, however, is one of the oldest facts of biology. Except for bacteria, nearly all life reproduces sexually at least some of the time, and two distinct sexes are generally necessary to do this.

Just why sex is such a popular method for transferring genes to the next generation is still a bit of an enigma, but it’s clear that distinct male and female sexes emerged multiple times throughout evolutionary history. It happened in the ancestors of plants and animals more than a billion years ago. That’s too far back for us to recover even sketchy details about how the original distinction between males and females evolved. Fortunately for us, we have an “evolutionary time machine” of sorts: the volvocine green algae. It’s a family of present-day species that nicely illustrates the evolutionary transition from a single-celled organism without very distinct sexes, to a multi-cellular one with genuine males and females.

Volvocine algae are like a time machine because, in the relatively brief period of 200 million years, this group evolved from a free-living, single-cell ancestor into a variety of multi-cellular life forms. To study this evolutionary process, biologists can compare a present-day single-cell species, Chlamydomonas reinhardtii, with its much larger, multi-cellular relative, Volvox carteri. Volvox has males and females, while Chlamydomonas doesn’t; by comparing the two, we can learn about how sexes evolve.

Chlamydomonas sex is typical for a single-cell sexual organism: primitive. These algae come in two different “mating types,” called “plus” and “minus.” Instead of issuing specialized male and female reproductive cells, this organism transforms its entire one-celled self into a gamete and seeks out a partner of the opposite mating type. Like two poles of a magnet, “plus” and “minus” organisms aren’t that different from each other. The differences that do exist serve mainly to allow one mating type to recognize and fuse with the other.

Volvox sex, on the other hand, is surprisingly familiar. These algae, made up of about 2,000 cells, exist as distinct males and females. The males produce sperm that fertilize the eggs of the females, producing a zygote that develops into an embryo. Sound familiar? But here’s the stunning fact about it: This whole reproductive process evolved from scratch in algae within the last 200 million years, during a time when reptiles, amphibians, mammals—descended from a long line of sexually reproducing ancestors—were roaming the Earth. The two sexes of Volvox are an evolutionary rerun.

SO HOW DO YOU get from mating types to males and females? That’s the question asked by a trio of researchers, at the Danforth Plant Science Center in St. Louis and the Salk Institute in La Jolla, in a study published this summer. The scientists began from the observation that distinct sexes have evolved repeatedly in life’s history, and the result is nearly always the same: females who produce relatively few large, immobile eggs, and males who produce many small, mobile sperm. To understand the genetic basis of Volvox males and females, the researchers tried swapping genes between the sexes.

They were interested in one gene in particular, called MID. Male Volvox have this gene, while the females don’t. This gene exists in single-celled algae as well, where it acts as a master mating type switch that prevents “minus” from turning into “plus.” The scientists reasoned that MID might do something similar in Volvox. They transferred a copy of this male-specific gene into females, which became pseudo-males and started making sperm. And when they deleted MID from the males, the algae became pseudo-females and started making eggs. Their results show that this master switch gene “control[s] two very different manifestations of sexual reproduction.” This gene was reprogrammed from a simple regulator of primitive mating types into one that controls the major differences between females and males.

The oldest and most fundamental way that males and females differ is in their reproductive cells. Once you have sex-specific reproductive cells, new sex-specific evolutionary strategies come into play. These drive the development of even more physical and behavioral differences between males and females. New genes fall under the control of the master switch to become sex-specific genes. In Volvox, about a dozen genes are found only in males or females. In humans, there are about 80 protein-coding genes on the Y chromosome that are specific to men. The human master switch is called SRY, and like MID in Volvox, its primary job is to switch on the genetic program to produce sperm.

There is no doubt that the trend in human societies is to exaggerate the differences between men and women—typically by emphasizing the supposedly lesser capabilities of women. Then society changes, and sex differences that many people took for granted as biological turn out to be social after all. Certainly compared to many species, the differences between human males and females are small. But those biological differences drive so much of our social behavior, for better and for worse, and the case of Volvox algae show how the differences between men and women probably began.

Michael White
Michael White is a systems biologist at the Department of Genetics and the Center for Genome Sciences and Systems Biology at the Washington University School of Medicine in St. Louis, where he studies how DNA encodes information for gene regulation. He co-founded the online science pub The Finch and Pea. Follow him on Twitter @genologos.

More From Michael White
Related Stories


Wednesday, May 7, 2014

Sexual Similarity Studies Get Framed as a Major New Finding of Sex Differences


From Slate, looks at how two new studies that identified sex similarities between men and women got reported in the media as offering major new findings in sex differences. How does sh!t like this happen so often?

As we get deeper and deeper into the human genome and are able to identify specifics in the male and female genome, we are likely to discover some real differences that impact, physical and mental health, as well as the development of body and mind.

Yet, even now, we are also learning of the incredible similarities in males and females. The studies discussed below (here is a link to one of them, Nature) found that there are 12 important genes on the Y chromosome that are important in controlling that state of the genome and the activation of other genes.

The New York Times (as well as others) presented these findings as representing "a fundamental difference in how the cells in men’s and women’s bodies read off the information in their genomes.” However, the Nature studies clearly demonstrated the opposite:
The 12 genes residing on the Y chromosome exist to ensure sexual similarity. The genes are “dosage-sensitive,” meaning that two copies are needed for them to function properly. We’ve long known that those 12 genes exist on X chromosomes. Females have the 12 genes active on both of their X chromosomes. If males, who have just one X, didn’t have them on the Y, they would not have a sufficient dosage of those genes. Now we know they do. Just like women.
Not only does this call into question how science gets reported in the media (either ignorance or an agenda seems to play a powerful role), but it also requires readers to be very skeptical when we see headlines about sex differences in men and women.

Sarah Richardson is the author of Sex Itself: The Search for Male and Female in the Human Genome.

Y All the Hype?

A study about sexual similarity gets framed as a major new finding of sex difference.

By Sarah S. Richardson



Illustration by Natalie Matthews-Ramo

Last month two Nature studies on the Y chromosome were in the news, trumpeted as revealing “differences in men’s and women’s bodies, differences found as deep down as the cellular level.” The coverage of the studies offers an allegory for our age about the way scientific hype and a fascination with the sex binary continue to influence scientific research on sex today.

The New York Times reported that scientists had discovered 12 genes on the Y chromosome that play “high-level roles in controlling the state of the genome and the activation of other genes.” They “may represent a fundamental difference in how the cells in men’s and women’s bodies read off the information in their genomes.” The Huffington Post quoted one of the studies’ authors as saying that these “special” genes “may play a large role in differences between males and females.”

Yet what the Nature articles actually show is the exact opposite. The 12 genes residing on the Y chromosome exist to ensure sexual similarity. The genes are “dosage-sensitive,” meaning that two copies are needed for them to function properly. We’ve long known that those 12 genes exist on X chromosomes. Females have the 12 genes active on both of their X chromosomes. If males, who have just one X, didn’t have them on the Y, they would not have a sufficient dosage of those genes. Now we know they do. Just like women.

Reports of newly found sex differences in the genome need to be viewed with healthy skepticism.

Furthermore, the 12 genes do not specialize in sex differences. The studies demonstrate that they are part of a family of genes that play an all-purpose regulatory role in the human genome. Scientists don’t yet know precisely what the genes do, but the studies show that they are important, because fetal viability is impaired without two doses of them.

How did a study of gene dosage equalization between males and females get framed as a major new finding of sex difference?

A little literary forensics reveals the story. In the very last lines of one of the Nature papers—the part of a paper where researchers typically engage in a bit of speculation—the scientists wonder if the X-derived and Y-derived versions of the proteins encoded by the 12 genes might “exhibit subtle functional differences.” They venture that if this is the case, the possibility of a role in sex differences in disease might be explored in the future.

And with that, the study’s most speculative moment became the headline.

Genetic sex difference claims will proliferate in the coming years, as more studies based on the genome come out. Yet reports of newly found sex differences in the genome need to be viewed with healthy skepticism and an awareness of how gender beliefs can distort our interpretation of scientific results.

This rush to see sex differences where they may not exist is nothing new. A 2005 Nature paper declared that the sexes differ at up to 350 genes on the X chromosome, a finding that garnered major media coverage and led one commentator to gush that “women and men differ genetically almost as much as humans differ from chimpanzees.” Follow-up studies confirmed only nine such genes—but no headlines touted the corrective.

A 2007 paper in the Journal of the American Medical Association reanalyzed 188 claims of genetic sex differences in recent peer-reviewed scientific articles and found that 55.9 percent were not statistically significant. Additionally, almost none of the findings of sex differences had been replicated by other studies—a critical measure of the validity of genomic findings. The authors concluded that in genetic sex difference research, “investigators very often seem to fall into classic traps.”

Last month’s Y chromosome studies show the continuing, stubborn influence of what I call the “sex difference paradigm.” The studies presented the unsexy claim that certain genes on the Y chromosome work to ensure sexual similarity. Filtered through our gender scripts and scientific hype generator, it became a revolutionary finding said to have groundbreaking implications for our understanding of the genetic basis of sex differences.

How can we break the difference paradigm? Top scientists such as Randy Schekman have recently drawn attention to the pernicious role of leading journals such as Nature in encouraging scientists to make big media-ready claims that later don’t hold up scientifically. But hype is only part of the problem. When it comes to sex, scientific reviewers, journals, funders, and reporters simply find similarities less interesting than differences.

What can be done to change that? A project at Stanford University is leading the way, working to “identify gender bias and understand how it operates in science and technology.” The Gendered Innovations initiative, funded in part by the National Science Foundation, is all about showing how critical analysis of gender assumptions can contribute to scientific knowledge. Now the challenge is filtering that understanding to the media and to the public so that we all bring some skepticism to too-tidy findings, and recognize that the real discoveries happen when we free ourselves from old mindsets.

~ Sarah S. Richardson is an assistant professor at Harvard University. She is the author of Sex Itself: The Search for Male and Female in the Human Genome.

Thursday, July 18, 2013

Fathers Pass Obesity to Their Offspring (and Their Offspring)

Here is yet another reason for men to stay fit and healthy (besides reducing the risks of cancer, heart disease, diabetes, arthritis, and cognitive diseases) - the sperm of obese men pass on obesity genes to their children and grandchildren. If you won't or can't commit to fitness for yourself, do it for your children and grandchildren.

Dad's sperm passes obesity on


THE UNIVERSITY OF ADELAIDE
TUESDAY, 16 JULY 2013

The sperm of an obese father can increase the risk of the next two generations being obese, even if they're eating healthily.


New research from the University of Adelaide shows that the sperm of obese fathers could increase the risk of both their children and their grandchildren to inherit obesity.

In laboratory studies, researchers from the University's Robinson Institute have found that molecular signals in the sperm of obese fathers can lead to obesity and diabetes-like symptoms in two generations of offspring, even though the offspring are eating healthily.

The results of the research are published online in The FASEB Journal.

"A father's diet changes the molecular makeup of the sperm. With obese fathers, the changes in their sperm - in their microRNA molecules - might program the embryo for obesity or metabolic disease later in life," says the lead author of the paper, Dr Tod Fullston, who is an NHMRC Peter Doherty Fellow with the University's Robinson Institute, based in Dr Michelle Lane's Gamete and Embryo Biology Group.

"For female offspring, there is an increased risk of becoming overweight or obese. What we've also found is that there is an increased chance of both male and female offspring developing metabolic disease similar to type 2 diabetes.

"This is the first report of both male and female offspring inheriting a metabolic disease due to their father's obesity," he says.

The study also extended into the second generation of progeny, which showed signs of similar metabolic disorders, including obesity, although it was not as severe as the first generation.

Dr Fullston says even if the obese father does not show any signs of diabetes, metabolic disease similar to diabetes was being seen in two generations of their descendants.

"It's been known for some time that the health of a mother before, during and after pregnancy can impact on her child's health, but the father's health during this period is often overlooked," Dr Fullston says.

"If our laboratory studies are translatable to humans, this could be a new and as yet unexplored intervention window into the epidemic of childhood obesity.

"A focus on the mother's health is extremely important, but we're seeing that the father's health is also important for conception. It's possible that by showing additional attention to diet and exercise in the father, this could have a positive impact on his future children and grandchildren."

~ Editor's Note: Original news release can be found here.