DOCSLIB.ORG

Development Team

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Development Team Paper No. : 01 Physical/ Biological Anthropology Module : 31 Applied Human Genetics Development Team Prof. Anup Kumar Kapoor Principal Investigator Department of Anthropology, University of Delhi Prof. Subho Roy Paper Coordinator Department of Anthropology ,University of Calcutta Dr. Sanjenbam Yaiphaba Meitei Content Writer Department of Anthropology, Manipur University, Manipur Content Reviewer Prof. Barun Mukhopadhyay Indian Statistical Institute, Kolkata Prof. K.D.Sharma Department of Anthropology, Punjab University, Chandigarh 1 Physical/Biological Anthropology Anthropology Applied Human Genetics Description of Module Subject Name Anthropology Paper Name 01 Physical/Biological Anthropological Module Name/Title Applied Human Genetics Module Id 31 2 Physical/Biological Anthropology Anthropology Applied Human Genetics Contents of this unit Introduction 1. Population Variation 2. Medicine and Healthcare a) Genetic screening b) Genetic epidemiology 3. Personal Identification 4. Archaeogenetics Summary Learning Objectives What are the scopes of human genetics? What could be the role of genetic traits in population variation? How could the inter population variation leads to varied prognosis of complex disorders? What are the major areas of healthcare that human genetics can be applied for? What would be the effect of technological advancement in this subject matter especially in case of forensic application? What could be the source of genetic information from archaeological remains? 3 Physical/Biological Anthropology Anthropology Applied Human Genetics Introduction Genetics has become an important part of our daily life. As we know that genetics is about the inheritance of genes from parental generation to next generation and also it is associated with expression of phenotype from genotype. This basic concept of genetics can be applied to a number of basic or applied researches as such, or it can be controlled or modified to get the desired result so. In fact, the application of human genetics has become more broaden in the post genomic era. Applied genetic researches are usually carried out to dig upon practical problem or to implement for the better human society such as genetic predisposition of certain disease, solving the human evolutionary queries, forensic application etc. In this module, some of the important application of the same is discussed. 1. Population variation The concept of genetics has been applied in exploring the human genetic variation, and hence depicts the population history or evolutionary framework of biological species. Individuals in a Mendelian population share a common gene pool that can be traced back to their ancestors. Every population has its own genetic structure which can be defined as the distribution of alleles and genotypes in the population. Statistical inferences play a crucial role in reconstructing the evolutionary framework. The basic principle in this approach lies in the concept that evolution could be constructed by analyzing the multilocus genotype on a chromosome observed in populations and their inheritance within families (Race and Sanger, 1975). Genetic variations in both inter and intra populations are studied through certain selected genetic markers. Genetic markers can be either serological or biochemical traits. In the post human genome project, genomic markers are more considered as more reliable tools for studying human genetic variation. There are certain basic characteristics to be considered for genetic markers, such as locus specific, polymorphic and easily genotyped. It is through these genetic variations that one’s population structure can be determined, and at the same time inter or intra population variation can also be evaluated through certain statistical models. Phylogenetic relationship of the population can also be determined based on the genetic similarities and differences. Consequently, exploring human genetic variation has become one of the important applications of human genetics and thereby trying to give an insight on the human evolution and earliest migration. Moreover, the knowledge of human genetic variation can also be applied in understanding the roles of genetic variation in the development and progression of complex disorders all over the world 4 Physical/Biological Anthropology Anthropology Applied Human Genetics population. It is assumed that the patterns of genetic variation shed light on recombination, demography, admixture, and evolutionary selection in the human population, and thereby projecting the underlying genetic manifestation of the diseases varied population wise. Further, population heterogeneity may lead to spurious associations while examining the genetic role in disease progression. It is hereby noteworthy to mention that good knowledge of population genetics or population structure is much needed in understanding the genetic mechanism of disease progression which may differ from population to population (Meitei et al., 2012). 2. Medicine and Healthcare Genetic technology is now an important part of medicine, and its impact will continue to grow as information from genomics is analyzed and applied to the diagnosis and treatment of human diseases (Cummings, 2010). Genetics has a very important role in medical aspects thereby promoting healthcare; hence an independent discipline has been emerged as medical genetics. With the concept of one gene one enzyme, the importance of gene in development of Mendelian disorders or classical single gene disorders cannot be ignored, as diseases can result from altered proteins or too little or too much of a protein, or proteins made at the wrong place or time (Lewis, 2009). Moreover, various complex disorders are now considered as the consequences of the interaction of gene and environment, even the inherited ones are sensitive. Some of the application of genetics in medicine and healthcare could be analyzed as such: a) Genetic screening and counseling: Screening of various genetic disorders – both single gene and complex disorders is very much essential for the promotion of common healthcare. There are a number of inherited disorders which are lethal or sub-lethal. Screening of such lethal or sub-lethal disorders is one of the important applications of human geneticists. It is expected that millions of people worldwide are affected to such genetic disorders with over 10000 monogenic inherited disorders (http://www.who.int/genomics/public/geneticdiseases/en/index2.html) and every newborn has a 3% chance of having a genetic disorder, underscoring the need for tests that accurately diagnose heritable diseases at all stages of life (Lewis, 2009). These monogenic disorders may be autosomal or sex linked inheritance in either dominant or recessive patterns. Dominant inheritance will result into the expression of phenotype or disorders in question even in presence of only one copies of mutant allele. While for recessive traits, two copies of mutant alleles are needed to express the phenotypic trait. The concerns of human geneticists in this regard lies in the identification of early prognosis of such lethal or sub genetic traits especially among the newborns, and hence remedial measures can be planned through counseling. 5 Physical/Biological Anthropology Anthropology Applied Human Genetics Reasons to seek genetic counseling: Family history of abnormal chromosomes Elevated risk of single gene disorder Family history of multifactorial disorder Family history of familial complex disorders Genetic counseling sessions: Family history Pedigree construction Information provided on specific disorders, modes of inheritance, tests to identify at-risk family members Testing arranged, discussion of results Links to support groups, appropriate services Follow-up contact Figure 1: Flowchart indicating steps involved in Genetic Counseling (Lewis, 2009) Genetic counseling is the process by which the patients or relatives at risk of an inherited disorder are advised of the consequences and nature of the disorder, the probability of developing or transmitting it, and the options open to them in management and family planning. This complex process can be separated into diagnostic (the actual estimation of risk) and supportive aspects (Sequeiros et al., 2012). The person who is giving advice is the counselor and the person who is seeking is counselee. Counselors need special attention in case of monogenic recessive disorders such as cystic fibrosis, phenylketonuria etc. as the normal couple has the probability of giving birth to affected children in the condition that both are carriers of the disorders. Early prognosis of such disorders is very much essential for the babies. Besides the monogenic inherited disorders, the counselors also deals with the complex disorders and the probable interaction of environment and gene based on the incidence of family history of the disorder. Though the counselors talk about the causes and consequences of genetic disorders, it is the counselee who has to take the final decision in this matter. A counselor can’t insist the counselee to opt or decide in favour of him. 6 Physical/Biological Anthropology Anthropology Applied Human Genetics b) Genetic epidemiology: Genetic Structure Inter-Population variation Population Genetics Population Genetic Epidemiology Figure 2: Interrelationship of Population Genetics and Genetic Epidemiology through population structure and inter population variation Epidemiological studies is one of the another important application
Load more

Recommended publications
  • A Longitudinal Cline Characterizes the Genetic Structure of Human Populations in the Tibetan Plateau
    Dartmouth College Dartmouth Digital Commons Open Dartmouth: Published works by Dartmouth faculty Faculty Work 4-27-2017 A Longitudinal Cline Characterizes the Genetic Structure of Human Populations in the Tibetan Plateau Choongwon Jeong University of Chicago Benjamin M. Peter University of Chicago Buddha Basnyat Oxford University Maniraj Neupane Mountain Medicine Society of Nepal Geoff Childs Washington University in St. Louis See next page for additional authors Follow this and additional works at: https://digitalcommons.dartmouth.edu/facoa Part of the Biology Commons, and the Computational Biology Commons Dartmouth Digital Commons Citation Jeong, Choongwon; Peter, Benjamin M.; Basnyat, Buddha; Neupane, Maniraj; Childs, Geoff; Craig, Sienna; Novembre, John; and Di Rienzo, Anna, "A Longitudinal Cline Characterizes the Genetic Structure of Human Populations in the Tibetan Plateau" (2017). Open Dartmouth: Published works by Dartmouth faculty. 2500. https://digitalcommons.dartmouth.edu/facoa/2500 This Article is brought to you for free and open access by the Faculty Work at Dartmouth Digital Commons. It has been accepted for inclusion in Open Dartmouth: Published works by Dartmouth faculty by an authorized administrator of Dartmouth Digital Commons. For more information, please contact [email protected]. Authors Choongwon Jeong, Benjamin M. Peter, Buddha Basnyat, Maniraj Neupane, Geoff Childs, Sienna Craig, John Novembre, and Anna Di Rienzo This article is available at Dartmouth Digital Commons: https://digitalcommons.dartmouth.edu/facoa/2500
    [Show full text]
  • Human Evolution: Pathogen Influence on Human Genetic Variation
    RESEARCH HIGHLIGHTS Nature Reviews Genetics | AOP, published online 22 November 2011; doi:10.1038/nrg3134 HUMAN EVOLUTION Pathogen influence on human genetic variation Human population genetic variation study, the statistical framework that by pathogens were heavily enriched in is known to be influenced by envi- was developed by Fumagalli et al. genes that are associated with autoim- ronmental pressures. By developing a enabled them to correlate allele mune diseases, such as coeliac disease novel statistical framework, Fumagalli frequencies for 500,000 SNPs in 55 and type 1 diabetes. and colleagues have been able to distinct human populations with local The finding that pathogens have discern the relative contributions of environmental factors, such as diet, left such a strong mark on human environmental factors to evolution climate conditions and pathogen load. genomes is perhaps not surprising of genomes, and they found that local Consistent with previous studies, given the influence that pathogens pathogen diversity had the strongest the authors found a greater correla- have on the human lifespan. However, role in the selective process. tion of these environmental factors the trace left by these pathogens Recent genome-wide human with the frequencies of genic SNPs at autoimmune disease gene loci population genetic analyses have and nonsynonymous SNPs than with suggests an intriguing relationship revealed that genes involved in traits non-genic SNPs. After correcting between achieving protection against such as immune function, skin pig- for demography, they showed that infection and maintaining disease- mentation and metabolism are non- pathogen diversity has the strongest causing mutations neutrally evolving sequences and have influence on local genetic variance, Hannah Stower therefore been under the influence of and they detected about 100 human environmental pressures.
    [Show full text]
  • Global Clues to the Nature of Genomic Mutations in Humans
    INSIGHT POPULATION GENETICS Global clues to the nature of genomic mutations in humans An analysis of worldwide human genetic variation reveals the footprints of ancient changes in genomic mutation processes. AYLWYN SCALLY factors may reflect recent evolutionary events, Related research article Harris K, Pritchard particularly the divergence of human popula- JK. 2017. Rapid evolution of the human tions and their global dispersal within the last mutation spectrum. eLife 6:e24284. doi: 10. 100,000 years. One way to address this question would be 7554/eLife.24284 to collect genomic and other data for thousands of families, identify de novo mutations in each of the offspring, and then analyse the factors con- tributing to them. However, this approach is ll children inherit a mixture of chromo- extremely demanding in terms of the resources somal sequences from their parents, needed. Now, in eLife, Kelley Harris and Jona- A and although the copying process than Pritchard of Stanford University report how involved is extremely accurate, some errors they have taken an alternative occur. We refer to such errors as de novo (new) approach (Harris and Pritchard, 2017) that germline mutations, and when they are passed involved using a dataset of whole-genome on to subsequent generations, these mutations sequences for 2504 individuals from 26 different are the raw material on which natural selection populations around the world (Auton et al., works and the source of all genetic differences 2015). Consider that any genetic variant in this between populations and species. Most have dataset, even if it is found today in many individ- negligible or minor effects, but some on very uals, was once a de novo mutation in a single rare occasions are responsible for serious ancestor.
    [Show full text]
  • Human Genetic Variation Section 3 Learning Objectives
    Human Genetic Variation Section 3 Learning objectives • Describe differences in types of genetic variation and how they affect phenotypes. • Identify inheritance patterns of genotype-phenotype relationships. • Describe the differences and the pros and cons of sequencing vs genotyping. Zoom Poll Our Genome in Numbers 23 chromosome pairs 3.2 billion base-pairs (A,C,G,T) ~20,000 genes ~1.5% of the genome is coding DNA Genetic variation to phenotype variation The changes in DNA What we actually see (disease, trait) Single base change = Single Nucleotide Polymorphism/Variant (SNP/SNV) Genetic variant – changes in amino acid codons Synonymous mutation Nonsynonymous is usually worse than synonymous Nonsense mutation Nonsynonymous mutations Missense mutation Some missense mutations can be less bad Both polar Deletions/insertions “Frameshifts” Mutations happen all the time, with every replication Human genome mutation rate is ~1.1×10−8 per site per generation. Human genome is over 3 billion base pairs. Each genome: 3,000,000,000 sites Mutation rate: 0.000000011 errors/site How many new mutations do you expect in expect in each cell replication? Zoom Poll Sometimes we don’t change the protein itself… A gene includes a lot of DNA that doesn’t become protein A gene includes a lot of DNA that doesn’t become protein A variant here can change gene “expression” A gene includes a lot of DNA that doesn’t become protein Or here can change the “splice site” to make a different protein Zoom breakout – discuss Q1 Besides single base changes, what types of changes can we have? Genetic Variation – structural variation tandem repeats (Huntington’s disease) The normal function of huntingtin is unknown.
    [Show full text]
  • Human Pigmentation Variation: Evolution, Genetic Basis, and Implications for Public Health
    YEARBOOK OF PHYSICAL ANTHROPOLOGY 50:85–105 (2007) Human Pigmentation Variation: Evolution, Genetic Basis, and Implications for Public Health Esteban J. Parra* Department of Anthropology, University of Toronto at Mississauga, Mississauga, ON, Canada L5L 1C6 KEY WORDS pigmentation; evolutionary factors; genes; public health ABSTRACT Pigmentation, which is primarily deter- tic interpretations of human variation can be. It is erro- mined by the amount, the type, and the distribution of neous to extrapolate the patterns of variation observed melanin, shows a remarkable diversity in human popu- in superficial traits such as pigmentation to the rest of lations, and in this sense, it is an atypical trait. Numer- the genome. It is similarly misleading to suggest, based ous genetic studies have indicated that the average pro- on the ‘‘average’’ genomic picture, that variation among portion of genetic variation due to differences among human populations is irrelevant. The study of the genes major continental groups is just 10–15% of the total underlying human pigmentation diversity brings to the genetic variation. In contrast, skin pigmentation shows forefront the mosaic nature of human genetic variation: large differences among continental populations. The our genome is composed of a myriad of segments with reasons for this discrepancy can be traced back primarily different patterns of variation and evolutionary histories. to the strong influence of natural selection, which has 2) Pigmentation can be very useful to understand the shaped the distribution of pigmentation according to a genetic architecture of complex traits. The pigmentation latitudinal gradient. Research during the last 5 years of unexposed areas of the skin (constitutive pigmenta- has substantially increased our understanding of the tion) is relatively unaffected by environmental influences genes involved in normal pigmentation variation in during an individual’s lifetime when compared with human populations.
    [Show full text]
  • Human Genetic Variation and Disease
    Resource pack: Human genetic variation and disease Scottish Curriculum links Higher Biology: DNA and the Genome Unit Study of DNA and the genome. The Unit covers the key areas of structure of DNA; replication of DNA; control of gene expression; cellular differentiation; the structure of the genome; mutations; evolution; genomic sequencing. Personal genomics. Higher Human Biology: Human Cells Unit Structure and Replication of DNA, Gene Expression, Genes and Proteins in Health and Disease, Human Genomics. The Unit covers the key areas of structure and replication of DNA; gene expression; genes and proteins in health and disease, human genomics. Expression of genotype and protein production which allows study of mutations and disorders National 5 Biology: Multicellular Organisms Unit Reproduction, variation and inheritance; the need for transport and effects of life-style choices on animal transport and exchange systems. Resource pack contents This resource pack provides information on: Genetic variation/ DNA mutations Genetic basis of disease risk Human population cohort studies and methods Genes and Proteins in Health and Disease Human Genomics Expression of genotype and protein production For more information on obesity and diabetes, mentioned as example diseases here, another resource pack is available: www.sserc.org.uk/images/Biology/Higher_Human/SQA/Diabetes_final.pdf Page 1 Background Many common diseases are influenced by a combination of multiple genes and environmental factors and are therefore referred to as complex diseases. Because they can be caused by both genetic and environmental factors, complex diseases – such as asthma, stroke and diabetes - can be difficult to treat. In 1990, a massive international scientific project called The Human Genome Project was launched to determine the sequence of the building blocks/letters/nucleotides of the human DNA code - the entire human genome.
    [Show full text]
  • Basic Principles and Laboratory Analysis of Genetic Variation Jesus Gonzalez-Bosquet and Stephen J
    UNIT 2. BIOMARKERS: PRACTICAL ASPECTS CHAPTER 6. Basic principles and laboratory analysis of genetic variation Jesus Gonzalez-Bosquet and Stephen J. Chanock UNIT 2 CHAPTER 6 CHAPTER Summary With the draft of the human genome of their functional significance. agnostically using dense data sets and advances in technology, the Understanding the true effect of with billions of data points. These approach toward mapping complex genetic variability on the risk of developments have transformed diseases and traits has changed. complex diseases is paramount. the field, moving it away from the Human genetics has evolved into The importance of designing pursuit of hypothesis-driven, limited the study of the genome as a high-quality studies to assess candidate studies to large-scale complex structure harbouring clues environmental contributions, as well scans across the genome. Together for multifaceted disease risk with as the interactions between genes these developments have spurred a the majority still unknown. The and exposures, cannot be stressed dramatic increase in the discovery discovery of new candidate regions enough. This chapter will address of genetic variants associated with by genome-wide association studies the basic issues of genetic variation, or linked to human diseases and (GWAS) has changed strategies for including population genetics, as traits, many through genome-wide the study of genetic predisposition. well as analytical platforms and association studies (GWAS) (1). More genome-wide, “agnostic” tools needed to investigate the Already over 7400 novel regions of approaches, with increasing contribution of genetics to human the genome have been associated numbers of participants from high- diseases and traits. with more than 75 human diseases quality epidemiological studies are or traits in large-scale GWAS (2).
    [Show full text]
  • Human Evolution Svante Pššbo
    David P. Bartel and Peter J. Unrau ¥ Early RNA-based life? Millennium issue kinase activity. Nature 371, 31Ñ36 44 Robertson, M.P. and Ellington, A.D. (1999) optimum. Proc. Natl. Acad. Sci. U. S. A. 94, 38 Jenne, A. and Famulok, M. (1998) A novel In vitro selection of an allosteric ribozyme 10612Ñ10617 ribozyme with ester transferase activity. that transduces analytes to amplicons. Nat. 50 Hager, A.J. and Szostak, J.W. (1997) Isolation Chem. Biol. 5, 23Ñ34 Biotechnol. 17, 62Ñ66 of novel ribozymes that ligate AMP-activated 39 Roth, A. and Breaker, R.R. (1998) An amino 45 Soukup, G.A. and Breaker, R.R. (1999) RNA substrates. Chem. Biol. 4, 607Ñ617 acid as a cofactor for a catalytic Engineering precision RNA molecular 51 Chapman, K.B. and Szostak, J.W. (1995) polynucleotide. Proc. Natl. Acad. Sci. U. S. A. switches. Proc. Natl. Acad. Sci. U. S. A. 96, Isolation of a ribozyme with 59Ñ59 ligase 95, 6027Ñ6031 3584Ñ3589 activity. Chem. Biol. 2, 325Ñ333 40 Huang, F.Q. et al. (1998) RNA enzymes with 46 Walde, P. et al. (1994) OparinÕs reactions 52 Tuschl, T. et al. (1998) Selection in vitro of two small-molecule substrates. Chem. Biol. 5, revisited: Enzymatic synthesis of novel ribozymes from a partially randomized 669Ñ678 poly(adenylic acid) in micelles and self- U2 and U6 snRNA library. EMBO J. 17, 41 Tawfik, D.S. and Griffiths, A.D. (1998) Man- reproducing vesicles. J. Am. Chem. Soc. 116, 2637Ñ2650 made cell-like compartments for molecular 7541Ñ7547 53 Wilson, C. and Szostak, J.W. (1995) In-vitro evolution.
    [Show full text]
  • Evolution: Explosive Human Genetic Variation
    RESEARCH HIGHLIGHTS Brand X Brand EVOLUTION Explosive human genetic variation Understanding the extent, distribution and age of human protein-coding genetic variants across diverse populations allows fascinating insights into human population dynamics and the resultant evolutionary forces. Cataloguing and dating such variation will also allow us to understand the origin of the seemingly endless list of potential disease variants and to prioritize among them for further investigation. A recent study describes the sequencing of 15,336 genes in 4,298 individuals of European American and 2,217 individuals of African American ancestry, providing insights into a recent human population expansion and the associated evolution of disease variants. As a part of the US National Institutes of Health Heart, Lung and Blood Institute (NHLBI)-sponsored Exome Sequencing Project (ESP), Fu et al. identified 1,146,401 autosomal single-nucleotide variants (SNVs) in the sequenced exomes. They dated these using a simulation approach that modelled the data to different coalescence scenarios. The age of the SNVs was consistent with a modified ‘out-of-Africa’ model in which accelerated population growth began 5,115 years ago with the per-generation growth rate being higher in European Americans than in African Americans. The identification of an excess of rare variants in the data supported the occurrence of this population expansion. Furthermore, the authors estimate that 73% of all protein-coding variants occurred within the past 5,000 years. SNVs that were more than 50,000 years old were more often associated with African American samples, probably as a result of stronger genetic drift in European populations that is associated with the migration out of Africa.
    [Show full text]
  • The Nature of Human Biological and Genetic Variability - Robert J
    PHYSICAL (BIOLOGICAL) ANTHROPOLOGY - The Nature Of Human Biological And Genetic Variability - Robert J. Meier THE NATURE OF HUMAN BIOLOGICAL AND GENETIC VARIABILITY Robert J. Meier Department of Anthropology, Indiana University, Bloomington, IN 47405 USA Keywords: Anthropometry, human growth, secular trends, body composition, asymmetry, modern humans, human ancestors, racial classification, developmental plasticity, clines, adaptation, temperature stress, hypoxia, skin color, polygenic inheritance, heritability, classical markers, Mendelian genetics, population genetics, microevolutionary processes, molecular markers, genetic variation, evolutionary medicine, genomic medicine Contents 1. Introduction 1.1. Historical Background 1.2. Ancient Egypt 1.3. The World Discovered 2. Anthropometry: Measuring Morphological Variation 2.1. Background 2.2. Measuring Human Growth 2.3. Secular Trends 2.4. Body Composition 2.5. Asymmetry 2.6. Comparing Modern Humans 2.7. Measuring our Ancestors 2.8. Medical Application of Anthropometry 2.9. Ergonomic Applications 3. Race: Attempts to Classify Variation 3.1. Early Classification 3.2. Twentieth-Century Classification 3.3. Developmental Plasticity 3.4. From Fixity to Process and Variation 3.5. Clines 4. Adaptability and Variability 4.1. Background 4.2. Adapting to Extreme Temperatures 4.3. High Altitude Stress 4.4. Variation in Skin Color 4.4.1. Skin Color Cline 4.4.2. Solar Radiation as Selection Agent 4.4.3. Melanin Concentration and Folate 4.4.4. Decreased Melanin Concentration 4.4.5. Skin Color and Vitamin D Hypothesis 4.4.6. Polygenic Inheritance 4.4.7. Heritability 4.4.8. Summary ©Encyclopedia of Life Support Systems (EOLSS) PHYSICAL (BIOLOGICAL) ANTHROPOLOGY - The Nature Of Human Biological And Genetic Variability - Robert J. Meier 5.
    [Show full text]
  • Ancient Human Genomes Reveal a Hidden History of Strong Selection in Eurasia
    bioRxiv preprint doi: https://doi.org/10.1101/2020.04.01.021006; this version posted April 3, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Ancient human genomes reveal a hidden history of strong selection in Eurasia Yassine Souilmi1,a,*, Raymond Tobler1,a,*, Angad Johar1,10, Matthew Williams1, Shane T. Grey2,3, Joshua Schmidt1, João C. Teixeira1, Adam Rohrlach4,5, Jonathan Tuke4,6, Olivia Johnson1, Graham Gower1, Chris Turney7, Murray Cox8, Christian D. Huber1,b,*, Alan Cooper9,b,* 1Australian Centre for Ancient DNA, The University of Adelaide, Adelaide, SA 5005 2Transplantation Immunology Group, Immunology Division, Garvan Institute of Medical Research 3St Vincent's Clinical School, Faculty of Medicine, University of New South Wales, Darlinghurst, New South Wales, Australia 4ARC Centre of Excellence for Mathematical and Statistical Frontiers, The University of Adelaide, Adelaide, South Australia 5005, Australia 5Department of Archaeogenetics, Max Planck Institute for the Science of Human History, Jena, Germany 6School of Mathematical Sciences, The University of Adelaide, Adelaide, South Australia 5005, Australia 7Chronos 14Carbon-Cycle Facility and Palaeontology, Geobiology and Earth Archives Research Centre (PANGEA), University of New South Wales, Sydney, NSW 2052 8Statistics and Bioinformatics Group, School of Fundamental Sciences, Massey University, Palmerston North 4410, New Zealand 9South Australian Museum, Adelaide, SA 5005, Australia and BlueSky Genetics, PO 287, Ashton, SA 5137, Australia a These authors contributed equally bThese authors contributed equally *Correspondence: [email protected] (Y.S.), [email protected] (R.T.), [email protected] (C.D.H.), [email protected] (A.C.) 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.04.01.021006; this version posted April 3, 2020.
    [Show full text]
  • Evidence of High Genetic Variation Among Linguistically Diverse Populations on a Micro-Geographic Scale: a Case Study of the Italian Alps
    Journal of Human Genetics (2012) 57, 254–260 & 2012 The Japan Society of Human Genetics All rights reserved 1434-5161/12 $32.00 www.nature.com/jhg ORIGINAL ARTICLE Evidence of high genetic variation among linguistically diverse populations on a micro-geographic scale: a case study of the Italian Alps Valentina Coia1, Ilaria Boschi2, Federica Trombetta2, Fabio Cavulli1, Francesco Montinaro3,4, Giovanni Destro-Bisol3,4, Stefano Grimaldi1 and Annaluisa Pedrotti1 Although essential for the fine-scale reconstruction of genetic structure, only a few micro-geographic studies have been carried out in European populations. This study analyzes mitochondrial variation (651 bp of the hypervariable region plus 17 single- nucleotide polymorphisms) in 393 samples from nine populations from Trentino (Eastern Italian Alps), a small area characterized by a complex geography and high linguistic diversity. A high level of genetic variation, comparable to geographically dispersed European groups, was observed. We found a difference in the intensity of peopling processes between two longitudinal areas, as populations from the west-central part of the region show stronger signatures of expansion, whereas those from the eastern area are closer to the expectations of a stationary demographic state. This may be explained by geomorphological factors and is also supported by archeological data. Finally, our results reveal a striking difference in the way in which the two linguistically isolated populations are genetically related to the neighboring groups. The Ladin speakers were found to be genetically close to the Italian-speaking populations and differentiated from the other Dolomitic Ladins, whereas the German-speaking Cimbri behave as an outlier, showing signatures of founder effects and low growth rate.
    [Show full text]