
Science Resources RSS Feeds
|
 |
 |
 |
Chimpanzee study reveals genome variation hotspots
May 16, 2006
A tale of two species: Genome variation in humans and chimpanzees TEMPE, Ariz. - Researchers believe that dynamic regions of the human genome - "hotspots" in terms of duplications and deletions - are potentially involved in the rapid evolution of morphological and behavioral characteristics that are genetically determined.
Now, an international team of researchers, including a graduate student and an associate professor from Arizona State University, are finding similar hotspots in chimpanzees, which has implications for the understanding of genomic evolution in all species.
"We found that chimpanzees have many copy number variants - duplications or deletions of large segments of DNA - in the same regions of the genome as do humans. What this suggests is that some regions of the genomes are inherently unstable in both humans and chimpanzees," says George (P.J.) Perry, a Ph.D. anthropology student working with Anne Stone, an associate professor in ASU's School of Human Evolution and Social Change in the College of Liberal Arts and Sciences.
"This is a relatively new area of research and this is the first time this has been investigated on a genome-wide scale in a population sample of nonhuman primates," Perry says of the findings published May 15 in the online early edition of the journal Proceedings of the National Academy of Sciences (PNAS).
Perry, who is the study's lead author, says: "These copy number variants may be very significant from an evolutionary perspective, and they're important to study and understand. We talk about genetic diseases and cures, but first you have to find out that genetic differences such as copy number variants are there. And then you can study what they're involved in and what they mean from a morphological variation and disease standpoint."
Specifically, the study of the processes that lead to variations and mutations within a species can help researchers understand the evolution of copy number differences between species, Perry explains.
"Ultimately, we can use information about within-a-species variation to identify unusual patterns between species," he says. "This may highlight copy number differences between humans and chimpanzees that were somehow involved in the evolution of human-specific traits."
"This study is an important first step, not the ultimate answer, but an exciting first step in studying the evolution of copy number variant regions and their downstream implications for disease and phenotypic variation," Perry says.
In the study, researchers looked at the structural genomic variation in DNA samples of 20 wild-born male chimpanzees.
"We identified 355 copy number variants among the genomes of these 20 unrelated chimpanzees and found that the overall chimpanzee genetic diversity may be more extensive than was previously thought," Perry says.
"This research not only illustrates the importance of studying the genetic variation in other primates to understand our own genome better, but it can also shed light on the diversity and adaptations of our nearest relatives," says Stone, who is one of the study's senior co-authors, along with Charles Lee, an assistant professor in the Department of Pathology at Brigham and Women's Hospital, a teaching affiliate of Harvard Medical School.
Arizona State University
|
 |

|
Computational Genome Analysis: An Introduction (Statistics for Biology and Health)
by Richard C. Deonier (Author), Simon Tavaré (Author), Michael S. Waterman (Author)
Computational Genome Analysis: An Introduction presents the foundations of key problems in computational molecular biology and bioinformatics. It focuses on computational and statistical principles applied to genomes, and introduces the mathematics and statistics that are crucial for understanding these applications. The book is appropriate for a one-semester course for advanced undergraduate or beginning graduate students, and it can also introduce computational biology to computer scientists, mathematicians, or biologists who are extending their interests into this exciting field. This book features: Topics organized around biological problems, such as sequence alignment and assembly, DNA signals, analysis of gene expression, and human genetic variation ...
|

|
Theories of Population Variation in Genes and Genomes (Princeton Series in Theoretical and Computational Biology)
by Freddy Bugge Christiansen (Author)
This textbook provides an authoritative introduction to both classical and coalescent approaches to population genetics. Written for graduate students and advanced undergraduates by one of the world's leading authorities in the field, the book focuses on the theoretical background of population genetics, while emphasizing the close interplay between theory and empiricism. Traditional topics such as genetic and phenotypic variation, mutation, migration, and linkage are covered and advanced by contemporary coalescent theory, which describes the genealogy of genes in a population, ultimately connecting them to a single common ancestor. Effects of selection, particularly genomic effects, are discussed with reference to molecular genetic variation. The book is designed for students of...
|

|
Large Scale Genome Variation in Health and Disease
by Ad Geurts Van Kessel (Editor)
|
|
|
AMPLIFICATION: Study Uncovers Genome Variation.: An article from: Analytic Separations News
by Business Communications Company, Inc. (Publisher)
This digital document is an article from Analytic Separations News, published by Business Communications Company, Inc. on August 1, 2004. The length of the article is 426 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
Citation Details Title: AMPLIFICATION: Study Uncovers Genome Variation. Publication: Analytic Separations News (Newsletter) Date: August 1, 2004 Publisher: Business Communications Company, Inc. Volume: 2 Issue: 3 Page: NA
Distributed by Thomson...
|

|
The Human Genome: Features, Variations and Genetic Disorders
by Akio Matsumoto (Editor), Mai Nakano (Editor)
The sequencing of the human genome reveals our complete complement of genetic material. The sequenced human genome is one of the most international biomedical research projects ever, which is important in our current often all-too-fractured world. This book defines the function of all 'unknown' human genes, delineates the functional and phenotypic significance of human genetic variants in humans, and explores the functions of the vast non-genic regions of the human genome. Human genome sequencing has revealed a great opportunity to deeply investigate the biology and evolution of the sex chromosome pair at a more global level, allowing new frontiers in the genetics research, such as a detailed knowledge of the sequence and the gene content of these chromosomes. This book provides the most...
|
|
|
Guilt by association: whole-genome scans yield disease clues.(This Week): An article from: Science News
by B. Vastag (Author)
This digital document is an article from Science News, published by Thomson Gale on June 9, 2007. The length of the article is 564 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
Citation Details Title: Guilt by association: whole-genome scans yield disease clues.(This Week) Author: B. Vastag Publication: Science News (Magazine/Journal) Date: June 9, 2007 Publisher: Thomson Gale Volume: 171 Issue: 23 Page: 355(1)
Distributed by Thomson...
|

|
Genetic Variation: Methods and Protocols (Methods in Molecular Biology)
by Michael R. Barnes (Editor), Gerome Breen (Editor)
With the continuing advances in sequencing technologies and the availability of thousands of distinct human genomes, we are fast approaching the day when "personal genomes" become a standard study measure and a routine component of personal health records. In Genetic Variation: Methods and Protocols, expert researchers address the rising importance of genome variation, both at the level of the individual and in population-based studies of disease, with a collection of detailed protocols reflecting the nature and impact of genetic variation on human phenotypes. The contributions cover a majority of the most important forms of genetic variation studied today, including single nucleotide polymorphisms (SNPs), insertions/deletion (indels), copy number variation (CNVs), variable number...
|

|
Variation in the Human Genome (Novartis Foundation Symposia)
by CIBA Foundation Symposium (Author)
The mapping of human genes is proceeding rapidly, and genes associated with specific inherited diseases are being identified, often providing insight into the molecular cause of the disease. At the moment, however, little consideration is being given to the variation present in different human populations. This variation bears a record of the population history of our species and how this has been affected by diseases, ecological adaptations, and pharmacological and nutritional responses. Treatment of inherited diseases that involve several genes will require knowledge of the degree and nature of genetic variation present in a population. This book discusses methods of analysing population genetic data and how contemporary genetic heterogeneity arises during the evolution and migration of...
|
|
|
Variation in Human Genome. (book reviews): An article from: Human Biology
by John H. Relethford (Author)
This digital document is an article from Human Biology, published by Wayne State University Press on October 1, 1997. The length of the article is 651 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.
Citation Details Title: Variation in Human Genome. (book reviews) Author: John H. Relethford Publication: Human Biology (Refereed) Date: October 1, 1997 Publisher: Wayne State University Press Volume: v69 Issue: n5 Page: p739(2)
Article Type: Book Review
Distributed by Thomson...
|

|
Copy Number Variation and Disease: Reprint Of: Cytogenetic and Genome Research 2008, Vol. 123, No. 1-4
by Hildegard Kehrer-sawatzki (Editor), David N. Cooper (Editor)
|
|