Category: Biology (page 6 of 63)

the gay gene

Gay

Science magazine reports on a study lending support to the existence of a gene for homosexuality. The study, led by J. Michael Bailey and Alan Sanders, was published this week at Psychological Medicine. The scientists analyzed the genomes of 409 pairs of gay brothers from 384 different families. A genome-wide linkage scan led to the identification of two potential markers, one on chromosome Xq28 (which had been reported in a previous smaller study) and another in a region of chromosome 8. Bailey, for one, was surprised to find any linkage:

Bailey says he went into the project skeptical, largely because Hamer had studied just 38 pairs of gay brothers. “I thought that Dean did a fine but small study, but if I had to bet, I would have bet against our being able to replicate it.”

Samantha Allen at The Daily Beast is unimpressed:

If you don’t see gay people celebrating this news in the streets, understand that we’ve been hearing news about a potential biological basis for homosexuality for a long time now. In 1991, neuroscientist Simon LeVay suggested that small differences in the size of certain cell clusters in the hypothalamus could influence sexual orientation in men. In 1993, geneticist Dean Hamer published a paper in Science that claimed that genetic markers on the X chromosome could influence the development of a same-sex orientation in men…

As the discipline of genetics changed, so too did the scientific approach to homosexuality. In 2012, scientists examined the possibility that variations in hormone levels in the womb could influence the expression of genes that affect sexual orientation, a line of inquiry that falls under the emerging sub-discipline of epigenetics. The popular media, once so easily convinced by LeVay that homosexuality resulted from brain size and by Hamer that homosexuality was genetic, promptly changed its tune to declare that homosexuality was now epigenetic. Hooray? If it’s hard to get excited about these studies, it’s because, at this point, biological explanations for homosexuality are like iPhones—a new one comes out every year.

Bailey and Sanders acknowledge their work has limitations. Even the strongest linkage on Xq28 wasn’t statistically significant, and genome wide association studies are better at homing in on genes for a trait than the linkage study they performed this time:

Sanders admits that the strongest linkage identified from an isolated genetic marker on Xq28 doesn’t clear the threshold for significance. But he contends that the case is bolstered by neighboring markers, which appear to be shared at higher rates between pairs of gay brothers. “The convergence of the evidence pointed towards” Xq28 and chromosome 8, he asserts.

Bailey and Sanders may soon have more data to back their claim—or refute it. They are now working on a GWA study that includes genetic data from the just-published work plus DNA samples from more than 1000 additional gay men. Based on the results published this week, “it looks promising for there being genes in both of these regions,” Bailey says, “but until somebody finds a gene, we don’t know.”

Meanwhile, the New Scientist worries about the implications of the research:

On the one hand, if sexual orientation is something people are born with, and cannot change even if they want to – akin to skin colour or handedness – this should overturn the notion that people choose to be gay and could equally well choose not to be. That knowledge would help rebut those who suggest that gayness is the result of a morally unacceptable decision, or a psychological disorder. It might also help people who struggle to understand or declare their own homosexuality.

On the other, some could try to redefine homosexuality as a biological abnormality. There is no way to change people’s sexuality, but if key genes are found, it might be possible to detect homosexuality before birth, or to “cure” people by altering those genes.

ebola

An electron micrograph of an Ebola virus virion

An electron micrograph of an Ebola virus virion.

Ebola has been making lots of news this year, as the virus has popped up in several West African countries. We are in the midst of the largest and most widespread outbreak in history.

Fruit bats are the main carriers of the virus in nature. Initially, humans become infected with the ebola virus after contact with infected bats or any living or dead animals that have been infected by the bats. This contact is often thought to be from consumption of infected meat. After humans become infected, the disease spreads through contact with infected bodily fluids including sweat, saliva, urine and semen. Ebola is insidious, and in some cases can take up to 21 days after exposure before symptoms manifest. Symptoms include a sudden onset of flu-like fever, ache and fatigue followed by vomiting or diarrhea.

Sky News details why the virus is so deadly:

When ebola enters the body, it targets dendritic cells in the immune system. Normally, when a virus is detected, these cells tell other cells to produce antibodies. Ebola prevents that signal getting out. As far as the immune system knows, everything inside the body is fine. Left alone, ebola then begins replicating rapidly. It then spreads into the bloodstream, infecting the whole body. Cells start to break up and die, in huge numbers. That finally triggers the immune system, which kicks in – far too aggressively.

Ordinarily when you get sick, the body releases proteins called cytokines. Some of these cells tell your blood vessels to become more permeable. This is to let antibodies travel through the body more quickly to fight the disease. But once ebola has taken hold of your body, the immune system reacts much too aggressively – and launches a cytokine storm. This causes blood vessels to become far too permeable, and they leak. At the same time, the body’s blood clotting mechanisms also act abnormally. This causes internal and external bleeding and is why ebola is known as a haemorrhagic fever. It causes tissue damage and organ failure.

Though the disease is deadly, people do survive and countries can contain outbreaks. Survivors’ blood may contain antibodies that can be used to treat others suffering from the disease.

2014 nobel prizes

Nobel_medal

The Nobel prizes were awarded this week. Each year there are three science related awards in the fields of medicine, physics and chemistry.

In the field of medicine, the award went to John O´Keefe, May-Britt Moser and Edvard I. Moser for discovering the brain cells that make up our positioning system. In 1971 John O’Keefe discovered that when a rat was in a certain part of the room, one part of the hippocampus was always activated. When the rat was in other parts of a room there were different cells activated. He termed these cells “place cells” and determined that they formed a map. In 2005, the Mosers discovered what they called “grid cells”. These cells generated a coordinate system and aid in finding our way along paths. Read more about the physiology and medicine prize here.

This years physics medal went to the invention of LEDs and was awarded to Isamu Akasaki, Hiroshi Amano, and Shuji Nakamura. The three researchers contributed to the development of LED technology, which is prevalent in today’s telephones, lamps, and computers. LED lights emit brighter light than incandescent lights and for longer periods of time. Read more about the award at Scientific American. The press release is here.

The chemistry prize was awarded to Eric Betzig, Stefan Hell, and William Moerner for developing super resolved fluorescence microscopy. Researchers thought they were limited by the limit of diffraction when it came to resolving images under a microscope. The three Nobel recipients have developed technology that helped overcome this limitation and resolve images into the nanometer scale. Stefan Hell developed a technique called stimulated emission depletion microscopy or STED. Bezig and Moerner, working separately, performed the groundwork for the development of single molecule microscopy. You can read the press release here, and a more detailed description of high resolution microscopy here.

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