STUDY REVEALS NEW GENES FOR EXCESSIVE ALCOHOL DRINKING

[Date Prev][Date Next][Thread Prev][Thread Next][Date Index][Thread Index]

 



U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
http://www.niaaa.nih.gov/

EMBARGOED FOR RELEASE: Monday, April 17, 2006, 5:00 p.m. ET

CONTACT: NIAAA Press Office, 301-443-3860, jbowersox@xxxxxxxxxxxxx

STUDY REVEALS NEW GENES FOR EXCESSIVE ALCOHOL DRINKING

Researchers supported by the National Institute on Alcohol Abuse and
Alcoholism (NIAAA), part of the National Institutes of Health (NIH),
have identified new genes that may contribute to excessive alcohol
consumption. The new study, conducted with strains of animals that have
either a high or low innate preference for alcohol, provides clues about
the molecular mechanisms that underlie the tendency to drink heavily. A
report of the findings appears in the April 18, 2006 issue of
"Proceedings of the National Academy of Sciences".

"These findings provide a wealth of new insights into the molecular
determinants of excessive drinking, which could lead to a better
understanding of alcoholism," notes NIAAA Director Ting-Kai Li, M.D.
"They also underscore the value that animal models bring to the
investigation of complex human disorders such as alcohol dependence."

Mice that have been selectively bred to have either a high or low
preference for alcohol have been a mainstay of alcohol research for many
years, allowing investigators to study diverse behavioral and
physiological characteristics of alcohol dependence. In the current
study, NIAAA grantee Susan E. Bergeson, Ph.D., of the University of
Texas (UT) at Austin, and a multi-site team of scientists participating
in NIAAA's Integrative Neuroscience Initiative on Alcoholism (INIA) used
microarray techniques to study gene expression in the brains of these
animals. Microarrays are powerful tools that investigators use for
comprehensive analyses of gene activity.

"Microarrays allow us to look at the full complement of genes that are
active in the brains of animals bred to exhibit very different alcohol
drinking behaviors," said Dr. Bergeson, an Assistant Professor of
Neurobiology in UT's Waggoner Center for Alcohol and Addiction Research.
When a gene is activated, cellular machinery transcribes certain parts
of the gene's DNA into messenger RNA (mRNA), which is the body's
template for creating proteins. The complete set of transcribed mRNA in
a tissue is termed the "transcriptome."

Dr. Bergeson and her INIA colleagues examined brain transcriptomes of
nine strains of mice, each differing in their voluntary alcohol
consumption.

"By measuring total gene expression in brains of each of the mouse
models we could explore which transcripts are consistently changed in
different genetic models of high and low alcohol intake and thereby
define the transcriptional signatures of genetic predisposition to high
and low alcohol consumption," said Dr. Bergeson.

The researchers employed novel statistical techniques to identify nearly
4,000 differentially expressed genes between the high and low alcohol
drinking mouse strains and to narrow the focus to 75 primary candidate
genes. In addition, a comparison of the mouse data with human genetic
studies revealed that genes with significant expression differences
reside in chromosomal regions that previously were shown to be
associated with human alcoholism.

Numerous pathways, as well as genes whose functions are currently
unknown, may contribute to the genetic predisposition to drink high
amounts of alcohol, notes Dr. Bergeson. "Our results will allow us to
begin to focus on targets never previously implicated in excessive
drinking. For example, genetic studies have shown that chromosome 9
contains genes that may regulate alcohol consumption in mice. Our
analyses allowed us to narrow our focus from thousands of genes in that
region to twenty."

"This first microarray-based analysis of a behavioral trait reveals many
new research opportunities and exemplifies the rich collaborative
potential of NIAAA's INIA consortium," adds Dr. Li.

The National Institute on Alcohol Abuse and Alcoholism, part of the
National Institutes of Health, is the primary U.S. agency for conducting
and supporting research on the causes, consequences, prevention, and
treatment of alcohol abuse, alcoholism, and alcohol problems and
disseminates research findings to general, professional, and academic
audiences. Additional alcohol research information and publications are
available at www.niaaa.nih.gov.

The National Institutes of Health (NIH) -- "The Nation's Medical
Research Agency" -- includes 27 Institutes and Centers and is a
component of the U.S. Department of Health and Human Services. It is the
primary federal agency for conducting and supporting basic, clinical and
translational medical research, and it investigates the causes,
treatments, and cures for both common and rare diseases. For more
information about NIH and its programs, visit http://www.nih.gov.

-----------------------------------------------------------
Reference: Mulligan, MK, et al. Toward Understanding the Genetics of
Alcohol Drinking Through Transcriptome Meta-analysis. "Proceedings of
the National Academy of Sciences" 2006 103/16: 6368-6373.
-----------------------------------------------------------
  
##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/apr2006/niaaa-17.htm.

To subscribe (or unsubscribe) from this list, go to
http://list.nih.gov/cgi-bin/wa?SUBED1=nihpress&A=1.

[Index of Archives]     [CDC News]     [FDA News]     [USDA News]     [Yosemite News]     [Steve's Art]     [PhotoForum]     [SB Lupus]     [STB]

  Powered by Linux