Tuesday, June 15, 2010

Oh Crap. More Autism Genes.

There's been much excitement about the latest big genetic study into autism, published in Nature : the grandly titled Autism Genome Project, brought to you by a crack team of no fewer than 177 researchers.

For a good summary of the research take a look here, and for a longer account here. In a nutshell, the authors examined DNA from almost 1000 people with an autism spectrum disorder. They were looking for deletions and duplications of segments of DNA: so-called copy number variations (CNVs). A CNV could be anything from missing half a chromosome, down to having an extra copy of just a small part of a single gene.

It turned out that autistic cases carry more CNVs affecting genes, on average, than controls. The difference was small - just a 1.2-fold increase - but significant, and reassuringly, the extra CNVs were especially common in genes already known to be related to autism. The authors conclude that about 5% of cases of autism are likely caused by a single CNV of the type they studied. In almost all cases it was a different variant in a different gene - in other words, each case is genetically unique. Here's the gory details.

So we have new autism genes - dozens of them. But is that good news? Not really - with genes, it's not a case of the more the merrier. If there's just one gene for a disease, it's pretty easy to work out how it does it. Genes code for proteins. Proteins do stuff in cells. Follow the trail of causality from gene to protein to the impact on the body, and you've understood the disorder. Nowadays, with the help of modern genetics, you can do this in a few years.

There are several hundreds of these nice easy monogenetic diseases. For example, a few months ago I reported on a case report of a guy with complex neurological and psychiatric symptoms, caused by a single mutation in the gene for the enzyme sepiapterin reductase. All of his symptoms followed logically from that mutation. With autism, there are already many known genes; this study has found many more; more are implicated each year. Oh dear.

My suspicion is that a large proportion of all of the genes that control brain development - which is a lot - will turn out to be autism genes. The brain is amazingly complex. Thousands of genes work in synchrony build a "normal" brain. There are an awful lot of things that might not go according to plan.

Sometimes, the outcome is a rare and bizarre condition like holoprosencephaly. More often, the end result falls into one of a few common categories, like epilepsy and mental retardation (intellectual disability). There is no one gene for these disorders: they're just one of the things that happens when a gene goes wrong. I suspect that autism is another.

At present we have no clear idea what is different about autistic brains. If we did, we could probably predict which genes would be autism genes. For example, one theory of autism is that brain cells are too tightly packed. Suppose that's true (it's almost certainly not that simple), and suppose that one day, someone finds a gene, pushy, that causes developing brain cells to make little molecular spikes that push each other away. It would not take a genius to predict that a mutation that stops pushy working might cause autism.

Of course pushy mutations would only account for a small fraction of cases: plenty of other mutations would have the same eventual impact. The point is that if we understood the biology of autism in this way, we'd know which genes to look for; we wouldn't have to fish around the whole genome looking for all kinds of random mutations.


It's true, as the authors of the Nature paper say, that genes can themselves provide clues as to the nature of the disease. They present a neat diagram of the functional relationships between their autism genes - what they do inside cells. But this is painted with a very broad brush - "cell adhesion" i.e. how cells fit together; "central nervous system development"; "cell proliferation".

This is why I'm personally more interested in research into the psychology and the neuroscience of autism than I am by the genetics. Genetic studies are important but there are glaring gaps in our knowledge that probably deserve at least as much attention.

Just for starters, there have been very few studies simply comparing the brains of autistic people to non-autistic controls at autopsy. I think in total there have been published post mortem reports on maybe 30 or 40 autistic brains...ever. Some very interesting results have emerged, but with such small numbers it's impossible to know what's really going on, especially since most of the cases also suffered other conditions, such as - no surprise - epilepsy and mental retardation. We need more autistic people to donate their brains to science, and more scientists to study them.

ResearchBlogging.orgPinto, D. et al. (2010). Functional impact of global rare copy number variation in autism spectrum disorders Nature DOI: 10.1038/nature09146

Oh Crap. More Autism Genes.

There's been much excitement about the latest big genetic study into autism, published in Nature : the grandly titled Autism Genome Project, brought to you by a crack team of no fewer than 177 researchers.

For a good summary of the research take a look here, and for a longer account here. In a nutshell, the authors examined DNA from almost 1000 people with an autism spectrum disorder. They were looking for deletions and duplications of segments of DNA: so-called copy number variations (CNVs). A CNV could be anything from missing half a chromosome, down to having an extra copy of just a small part of a single gene.

It turned out that autistic cases carry more CNVs affecting genes, on average, than controls. The difference was small - just a 1.2-fold increase - but significant, and reassuringly, the extra CNVs were especially common in genes already known to be related to autism. The authors conclude that about 5% of cases of autism are likely caused by a single CNV of the type they studied. In almost all cases it was a different variant in a different gene - in other words, each case is genetically unique. Here's the gory details.

So we have new autism genes - dozens of them. But is that good news? Not really - with genes, it's not a case of the more the merrier. If there's just one gene for a disease, it's pretty easy to work out how it does it. Genes code for proteins. Proteins do stuff in cells. Follow the trail of causality from gene to protein to the impact on the body, and you've understood the disorder. Nowadays, with the help of modern genetics, you can do this in a few years.

There are several hundreds of these nice easy monogenetic diseases. For example, a few months ago I reported on a case report of a guy with complex neurological and psychiatric symptoms, caused by a single mutation in the gene for the enzyme sepiapterin reductase. All of his symptoms followed logically from that mutation. With autism, there are already many known genes; this study has found many more; more are implicated each year. Oh dear.

My suspicion is that a large proportion of all of the genes that control brain development - which is a lot - will turn out to be autism genes. The brain is amazingly complex. Thousands of genes work in synchrony build a "normal" brain. There are an awful lot of things that might not go according to plan.

Sometimes, the outcome is a rare and bizarre condition like holoprosencephaly. More often, the end result falls into one of a few common categories, like epilepsy and mental retardation (intellectual disability). There is no one gene for these disorders: they're just one of the things that happens when a gene goes wrong. I suspect that autism is another.

At present we have no clear idea what is different about autistic brains. If we did, we could probably predict which genes would be autism genes. For example, one theory of autism is that brain cells are too tightly packed. Suppose that's true (it's almost certainly not that simple), and suppose that one day, someone finds a gene, pushy, that causes developing brain cells to make little molecular spikes that push each other away. It would not take a genius to predict that a mutation that stops pushy working might cause autism.

Of course pushy mutations would only account for a small fraction of cases: plenty of other mutations would have the same eventual impact. The point is that if we understood the biology of autism in this way, we'd know which genes to look for; we wouldn't have to fish around the whole genome looking for all kinds of random mutations.


It's true, as the authors of the Nature paper say, that genes can themselves provide clues as to the nature of the disease. They present a neat diagram of the functional relationships between their autism genes - what they do inside cells. But this is painted with a very broad brush - "cell adhesion" i.e. how cells fit together; "central nervous system development"; "cell proliferation".

This is why I'm personally more interested in research into the psychology and the neuroscience of autism than I am by the genetics. Genetic studies are important but there are glaring gaps in our knowledge that probably deserve at least as much attention.

Just for starters, there have been very few studies simply comparing the brains of autistic people to non-autistic controls at autopsy. I think in total there have been published post mortem reports on maybe 30 or 40 autistic brains...ever. Some very interesting results have emerged, but with such small numbers it's impossible to know what's really going on, especially since most of the cases also suffered other conditions, such as - no surprise - epilepsy and mental retardation. We need more autistic people to donate their brains to science, and more scientists to study them.

ResearchBlogging.orgPinto, D. et al. (2010). Functional impact of global rare copy number variation in autism spectrum disorders Nature DOI: 10.1038/nature09146

Monday, June 14, 2010

BOM DIA A TODOS!!!!

bomdia_132.gif

ESTAMOS EM FESTA DE COPA DO BRASIL!!!
VAMOS TORCER E GANHAR ESTA COPA
Meu querido amigo Ivan deixou esta letra.
orkut e hi5, Brasileiras, brasil, mapa do brasil, onça, bandeira do  brasil
VAMOS VER...

Vamos todos juntos
pra frente Brasil
Salve a Seleção !!
Novamente é aquela
corrente pra frente
em verde e amarelo
Brasil é emoção
todos juntos vamos
pra frente Brasil
Brasil, Brasil
Salve a Seleção !!



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TEM SELINHO PRÊMIO DE QUALITY.

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The Face of a Mouse in Pain

Have you ever wanted to know whether a mouse is in pain?

Of course you have. And now you can, thanks to Langford et al's paper Coding of facial expressions of pain in the laboratory mouse.

It turns out that mice, just like people, display a distinctive "Ouch!" facial expression when they're suffering acute pain. It consists of narrowing of the eyes, bulging nose and cheeks, ears pulled back, and whiskers either pulled back or forwards.

With the help of a high-definition video camera and a little training, you can reliably and accurately tell how much pain a mouse is feeling. It works for most kinds of mouse pain, although it's not seen in either extremely brief or very long-term pain.

Langford et al tried it out on mice with a certain genetic mutation, which causes severe migraines in humans. These mice displayed the pain face even in the absence of external painful stimuli, showing that they were suffering internally. A migraine drug was able to stop the pain.

Finally, lesions to a part of the brain called the anterior insula stopped mice from expressing their pain. This is exactly what happens in people as well, suggesting that our displays of suffering are an evolutionary ancient mechanism. Of course this kind of study can't prove that animals consciously feel pain in the same way that we do, but I see no reason to doubt it: we feel pain as a result of neural activity, and mammals have exactly the same brain systems.

ResearchBlogging.orgLangford, D., Bailey, A., Chanda, M., Clarke, S., Drummond, T., Echols, S., Glick, S., Ingrao, J., Klassen-Ross, T., LaCroix-Fralish, M., Matsumiya, L., Sorge, R., Sotocinal, S., Tabaka, J., Wong, D., van den Maagdenberg, A., Ferrari, M., Craig, K., & Mogil, J. (2010). Coding of facial expressions of pain in the laboratory mouse Nature Methods, 7 (6), 447-449 DOI: 10.1038/nmeth.1455

The Face of a Mouse in Pain

Have you ever wanted to know whether a mouse is in pain?

Of course you have. And now you can, thanks to Langford et al's paper Coding of facial expressions of pain in the laboratory mouse.

It turns out that mice, just like people, display a distinctive "Ouch!" facial expression when they're suffering acute pain. It consists of narrowing of the eyes, bulging nose and cheeks, ears pulled back, and whiskers either pulled back or forwards.

With the help of a high-definition video camera and a little training, you can reliably and accurately tell how much pain a mouse is feeling. It works for most kinds of mouse pain, although it's not seen in either extremely brief or very long-term pain.

Langford et al tried it out on mice with a certain genetic mutation, which causes severe migraines in humans. These mice displayed the pain face even in the absence of external painful stimuli, showing that they were suffering internally. A migraine drug was able to stop the pain.

Finally, lesions to a part of the brain called the anterior insula stopped mice from expressing their pain. This is exactly what happens in people as well, suggesting that our displays of suffering are an evolutionary ancient mechanism. Of course this kind of study can't prove that animals consciously feel pain in the same way that we do, but I see no reason to doubt it: we feel pain as a result of neural activity, and mammals have exactly the same brain systems.

ResearchBlogging.orgLangford, D., Bailey, A., Chanda, M., Clarke, S., Drummond, T., Echols, S., Glick, S., Ingrao, J., Klassen-Ross, T., LaCroix-Fralish, M., Matsumiya, L., Sorge, R., Sotocinal, S., Tabaka, J., Wong, D., van den Maagdenberg, A., Ferrari, M., Craig, K., & Mogil, J. (2010). Coding of facial expressions of pain in the laboratory mouse Nature Methods, 7 (6), 447-449 DOI: 10.1038/nmeth.1455

Saturday, June 12, 2010

COPA DO MUNDO!!!!!VAMOS LÁ BRASIL...

bomdia_132.gif

1amizade29.jpg


EM ÉPOCA DE COPA, TUDO VALE A PENA DE SER CONSTRUINDO..
O IMPORTANTE É PARTICIPARM E REALIZAR.
UM LINDO CARTAZ REALIZADO NA ESCOLA.

OBRIGADA ELÔ, POR COMPARTILHAR CONOSCO, SEU LINDO TRABALHO.PARABÉNS AMIGA. SEMPRE DEDICADA E CARINHOSA COM TUDO O QUE FAZ E REALIZA.
APRENDEMOS MUITO, UM COM O OUTRO..



APROVEITO AINDA PARA DIZER A TODOS...

ESTE LIVO É A MINHA PAIXÃO.. NADA MELHOR QUE ELE PARA LEMBRAR O DIA DOS NAMORADOS.


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Friday, June 11, 2010

ASSIM SE CULTIVA...

NOSSA AMIZADE É ASSIM..
f055.bmp

SE VOCÊ AINDA NÃO LEVOU AS ROSAS..É SÓ LEVAR..UM GRNADE ABRAÇO.

FIZ COM MUITO CARINHO...



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