Cellular and Animal Models in Human Genomics Research

• Editore: Academic Press
• Anno: 2019
• ISBN:
  9780128165744
• Argomento: Medicina
• Categoria: Genetica in medicina

Cellular and Animal Models in Human Genomics Research provides an indispensable resource for applying comparative genomics in the annotation of disease-gene associated variants that are identified by human genomic sequencing. The book presents a thorough overview of effective protocols for the use of cellular and animal modeling methods to turn lists of plausible genes into causative biomarkers. With chapters written by international experts, the book first addresses the fundamental aspects of using cellular and animal models in genetic and genomic studies, including in-depth examples of specific models and their utility, i.e., yeast, worms, flies, fish, mice and large animals.

Protocols for properly conducting model studies, genomic technology, modeling candidate genes vs. genetic variants, integrative modeling, utilizing induced pluripotent stem cells, and employing CRISPR-Cas9 are also discussed in-depth.

• Provides a thorough, accessible resource that helps researchers and students employ cellular and animal models in their own genetic and genomic studies
• Offers guidance on how to effectively interpret the results and significance of genetic and genomic model studies for human health
• Features chapters from international experts in the use of specific cellular and animal models, including yeast, worms, flies, fish, mice, and large animals, among other organisms

Chapter 1

Introduction to Human Genetics

Jennifer E. Posey¹ and Katherina Walz^2,3, ¹Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States, ²Department of Human Genetics, Miller School Medicine, University of Miami, Miami, FL, United States, ³John P. Hussman Institute for Human Genomics, University of Miami, Miami, FL, United States

Abstract

The last three decades have seen tremendous growth in the ability to link genes, and individual variants, to human disease traits. Genome-wide assays such as chromosomal microarray and exome and genome sequencing have stimulated this growth. Model organism studies are instrumental for understanding the molecular mechanisms underlying phenotypic expression associated with a particular locus, and enable a true dissection of both functional variant types and combinations of variants (biallelic or multilocus) on human disease traits. Below we review the current status of discovery in human genetics and genomics, and describe several examples of discoveries for which model organism study will provide a cornerstone for elucidating relationships between genomic variation, molecular pathogenesis of disease, and disease biology, with the potential to identify targets for therapeutic development and enable precision medicine.

Keywords

Chromosomal microarray; disease traits; exome sequencing; gene discovery; genome sequencing; model organisms; precision medicine

1.1 Introduction

The last three decades have seen tremendous growth in the ability to link genes, and individual variants, to human disease traits. Genome-wide assays such as chromosomal microarray and exome and genome sequencing have stimulated this growth. Model organism studies are instrumental for understanding the molecular mechanisms underlying phenotypic expression associated with a particular locus, and enable a true dissection of both functional variant types and combinations of variants (biallelic or multilocus) on human disease traits. Below we review the current status of discovery in human genetics and genomics, and describe several examples of discoveries for which model organism study will provide a cornerstone for elucidating relationships between genomic variation, molecular pathogenesis of disease, and disease biology, with the potential to identify targets for therapeutic development and enable precision medicine.

1.2 Current Status of Discovery

1.2.1 From 0 to 60: Linking Human Genetic and Genomic Variation to Human Disease

In many ways the discovery of the human chromosome number in 1956¹ formed the cornerstone on which our present understanding of the relationship between individual genomes and their impact on the expression of disease would be built. Karyotype technology led to the elucidation of common chromosomal aneuploidies underlying previously clinically characterized conditions such as Down syndrome, first described in 1866² but not characterized cytogenetically until 1959.³ The first disease gene would be mapped in 1983,⁴ eventually linking trinucleotide repeat expansions in huntingtin (HTT) to the expression of Huntington disease.⁵ From that time, both single-gene disorders and genomic disorders^6–8 resulting from submicroscopic structural variation of the human genome were increasingly described.

Linkage analysis and genome-wide association studies (GWAS) were used to identify common polymorphisms associated with a disease trait of interest, but they often fell short of directly identifying the disease gene and etiologic rare variant, necessitating additional techniques such as positional cloning for disease gene discovery. The development and implementation of tools that enable a direct genome-wide interrogation for rare structural and single nucleotide variants would revolutionize human disease gene discovery. In this regard, chromosomal microarray (CMA), exome sequencing (ES), and genome sequencing (GS) have truly accelerated gene discovery. Concurrent with technology development has been the elaboration of numerous variant annotation resources, including those that provide minor allele frequency data for populations of varying ethnicities, such as the Exome Aggregation Consortium (ExAC),⁹ the Genome Aggregation Database (gnomAD), the 1000 Genomes Project,¹⁰ the National Heart Lung and Blood Institute Exome Sequencing Project (http://evs.gs.washington.edu/EVS/), and the Atherosclerosis Risk in Communities¹¹ databases, as well as catalogs of human structural variation such as the Database of Genomic Variants (DGV) and the Database of Genomic Variation and Phenotype in Humans Using Ensembl Resources (DECIPHER). Measures of evolutionary conservation [GERP (Genomic Evolutionary Rate Profiling), phyloP] and estimates of protein functional impact [SIFT(Sorting Intolerant From Tolerant),¹² PolyPhen2 (Polymorphism Phenotyping v2),¹³ MutationTaster,¹⁴ LRT (Likelihood Ratio Test),¹⁵ CADD (Combined Annotation Dependent Depletion),¹⁶ REVEL (Rare Exome Variant Ensemble Learner)¹⁷] for identified variants have also improved genome-wide analytic methods. Bioinformatics approaches to genome-wide analyses have advanced our ability to interrogate large datasets, with rapid detection of copy number variants, de novo mutations, and absence of heterozygosity from exome and genome variant data,^18–23 as well as prediction tools such as the probability of loss-of-function (LoF) intolerance⁹ and the likelihood that a truncating variant will escape from nonsense-mediated decay.²⁴ Increasing use of expression catalogs, such as the Genotype-Tissue Expression database (GTEx), has also been harnessed to prioritize candidate disease genes through comparison of their tissue expression patterns to those of the disease trait of interest.²⁵

The development of genome-wide assays and a tremendous toolkit for genomic variant analyses has led to a time of rapid growth in our understanding of genetic variation and its impact on human health. Below we highlight recent accomplishments in the field of human genetics and genomics.

1.2.2 Mendelian Conditions

Rare disease has been defined as a disease trait impacting fewer than 200,000 individuals in the US population. Traditionally, these conditions are associated with variants that are rare in the population (well below 1%) and convey a large effect on trait manifestation. Such traits are often referred to as “Mendelian conditions,” as expression of the disease trait follows expected Mendelian modes of inheritance for a monogenic, or single locus, trait: autosomal dominant, autosomal recessive, X-linked, or mitochondrial. The diagnosis of a Mendelian condition can have immediate clinical impact, providing a molecular diagnosis and recurrence risk information for the affected family, and informing expectant medical management, and potentially therapeutic management, for the individual. This clinical value underscores the need for complete functional and phenotypic annotation of all ~20,000 genes in the human genome.

The current pace of human disease gene discovery for Mendelian conditions has never been greater and shows no evidence of slowing down. Despite this, to date, only 4083 genes (representing ~20% of the genes in the human genome) are cataloged in the Online Mendelian Inheritance in Man (OMIM) database as having one or more high-penetrance disease traits (www.OMIM.org; May 3, 2019). These data underscore both the high proportion of human genes that remain to be phenotypically annotated, and the complexity of gene–phenotype relationships, which do not always follow a one-to-one ratio.

Beyond simply the identification of novel disease genes underlying Mendelian conditions, a number of key discoveries have elucidated this very relationship between genes and their associated phenotypes. Traditional thinking led to a one gene-one disease model whereby a single gene or locus was associated with a particular disease trait, with inheritance following either a dominant or recessive pattern. However, there are increasing examples of gene–phenotype relationships that break with this traditional mold, underscoring the degree of allelic and locus heterogeneity, variability in penetrance and expression of disease traits, and combinatorial effects of rare variants at more than one locus in human disease. Genes such as RET may be associated with more than one disease trait, with rare constitutional variants leading to autosomal dominant multiple endocrine neoplasia type 2A (OMIM #171400) or the autosomal dominant neurocristopathy Hirschsprung disease (OMIM #142623). There are also increasing examples of genes associated with both dominant and recessive inheritance of disease traits. For some such genes, the dominantly inherited (due to monoallelic variation) trait is more severe (GJB2, KIF1A, MAB21L2, NALCN), whereas for other such genes the recessively inherited (due to biallelic variation) trait is more severe (AARS, CLCN1, EGR2, ROR2).²⁶ Monoallelic and biallelic variants in CLCN1 lead to the same disease trait: dominantly or recessively inherited myotonia congenita (OMIM #160800, #255700). In contrast, variants in ATAD3A consistently affect the neurologic system, but clinically observed phenotypes are distinct when the etiologic variant is monoallelic (developmental delay, axonal neuropathy, hypotonia, hypertrophic cardiomyopathy) or biallelic (developmental delay, hypotonia, ataxia, seizures, and congenital cataracts with cerebell...