Are Deafness Genes Spreading?

Levonian

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From the October 23, 2000 issue of sciencenow, an online publication of the American Association for the Advancement of Science.

Are Deafness Genes Spreading?

Philadelphia—Deafness may be becoming more common, according to a study presented here on 6 October at a meeting of the American Society of Human Genetics. The researchers believe increased opportunities for deaf people to meet and marry each other may lead to a rise in frequency of an important class of deafness causing mutations.

Gene mutations at more than 200 locations on the genome cause inherited deafness, which accounts for about half of deafness in general. Recently, clinical geneticists reported that faulty copies of a gene called Cx 26 cause about 35% of all cases of deafness.

That number seemed remarkably high to Walter Nance, a geneticist at Virginia Commonwealth University in Richmond. From a statistical analysis of data on 19th-century American families with deaf children, he estimated that in those days, Cx 26 mutations accounted for only 17% of inherited deafness. Nance reasoned that intermarriage might explain the increase in Cx 26 deafness, because two parents with this mutation will always have deaf children. Marriages among the deaf have been on the rise ever since the development of sign language and the establishment of schools for the deaf in the last 2 centuries.

To test this theory, Nance traveled to Mongolia, where intermarriage between the deaf is still relatively rare. There he collected DNA from about 100 deaf and 150 hearing people. As he suspected, very few of the deaf Mongolians had mutations in Cx 26.

Not everybody is convinced. "It's a reasonable hypothesis, because deaf people tend to marry deaf people," says David Kelsell, a geneticist at Queen Mary and Westfield College in London, United Kingdom. But he says Nance needs to repeat the study in other ethnic populations, because the frequency of Cx 26 mutations may have been different in Mongolians to begin with. Nance agrees; his lab has already begun looking at the frequency of Cx 26 mutations in Turkey.

If his theory is correct, Nance says, it would mean that intermarriage is not just increasing the percentage of deafness attributable to Cx 26, but also the overall frequency of deafness. So far, that has been hard to measure because there aren't good data on the occurrence of deafness in the past.
 
Cool. :-D SPREAD THE AWARENESS!

At least there is a possibilty that every person in the world will know or meet a deaf person at least once in their lifetime... and this may lead to remove the language barrier...

everybody needs to meet everybody else!
:wave: [greetings in various languages]
 
The abstract of Nance's paper:

Testing the Hypothesis that Assortative Mating has Increased the Frequency of Cx 26 Deafness. W.E. Nance1, X-Z. Liu1, R. Erdenetungalag2, J. Radnaabazar2, B. Dangaasuren2, A. Pandya1. 1) Dept Human Genetics, Virginia Commonwealth Univ, Richmond, VA; 2) Dept Maternal and Child Health, Ulaanbaatar, Mongolia.

Using a novel extension of segregation analysis, we have shown that the frequency of homozygosity for Connexin 26 (Cx 26) mutations among the deaf in the U.S. has increased from about 19% to 35% since 1800. We proposed the increasing frequency may be caused in part by the intense assortative mating for deafness in this country during that period (Lancet, in press). For a genetically heterogeneous recessive trait such as deafness, assortative mating preferentially increases the frequency of the commonest recessive genotype since these individuals account for a disproportionate share of the non-complementary matings that can only produce deaf offspring. To test our hypothesis, we screened for Cx 26 mutations in a sample of deaf Mongolian students who belong to a population without a long tradition of intermarriages among the deaf. At least half of the Mongolian population still lead a nomadic lifestyle; deaf students have been educated at a central school in Ulaanbaatar only since the mid 1950's; sign language was not introduced until 1994 and among 620 deaf probands at the school none had two deaf parents. Cx 26 testing has been completed by direct fluorescent sequencing of the coding exon in probands from 10 simplex and 18 multiplex sibships. Eleven were found to carry the V27I polymorphism, which has also been noted in other populations but no examples of the 35DelG mutation or any other pathologic allele was encountered. In contrast, the expected number of Cx 26(+) cases in a comparable U.S. sample would be 8(p<0.005). The low frequency of Cx 26(+) cases in a population where deaf marriages have been very uncommon in the past supports the view that assortative mating may explain the high frequency of this trait in other populations. Low Cx 26(+) rates in Japan and anecdotal reports from China and India are consistent with our data. If our hypothesis is correct, assortative mating may represent another important mechanism in addition to genomic instability and heterozygote advantage which can maintain specific phenotypes at unexpectedly high frequencies in the population.
 
gnarlydorkette said:
Cool. :-D SPREAD THE AWARENESS!

At least there is a possibilty that every person in the world will know or meet a deaf person at least once in their lifetime... and this may lead to remove the language barrier...

everybody needs to meet everybody else!
:wave: [greetings in various languages]

Not sure if your aware of this but... i'm pretty sure everyone will at 1 time or another in their life meet a deaf person, and just seeing or meeting 1 wont remove any barriers. Language barriers... thats another issue entirely, since there are over 200 languages on the planet, my guess is alot more.
 
OMG! We need to stop this! I'd hate to see the hearies breed out of existence!
 
VamPyroX said:
OMG! We need to stop this! I'd hate to see the hearies breed out of existence!
The elvoution of deafness has already begun... :twisted:
 
Y said:
hmm, you forgot one more thing to add this:

"Just open your legs and give till it hurts" haha...


pervert
 
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