Clinical review

Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases

David J Weatherall. 

Institute of Molecular Medicine, John Radcliffe Hospital, Oxford OX3 9DS

As a result of the revolution in the biological sciences following the development of recombinant DNA technology and the sequencing of most of the human genome, the role of genetics in the pathogenesis of human disease now dominates biomedical research. There is every sign that the rapidly evolving technology of the post genome era will unravel the function of the human genome and explain how the 50 000 to 100 000 genes interact with one another and the environment to make us what we are.

The central question for the medical sciences is the extent to which it will be possible to relate events at the molecular level with the clinical findings or phenotypes of patients with particular diseases. This problem will permeate every aspect of medical research and practice in the future. It will dominate predictive genetics and genetic counselling. It will also be of major importance for clinical decision making as new and novel approaches to the treatment of disease become available, particularly those involving genetic manipulation. Further exploration of the genome may also provide information on some of the common killers of Western society, such as heart disease, stroke, diabetes, and psychiatric disease, leading to a new form of pharmacology in which drugs are tailored to an individual's genetic make up. Even more important, and certainly more complex, will be relating genotype to phenotype. Many of our most important diseases almost certainly reflect varying susceptibility, due to the action of many different genes and a wide variety of environmental factors and to the ill understood biology of ageing.

Is there any way of guessing the likely levels of complexity that will be encountered as the genetic basis of disease is explored with the new technology? Theoretically, monogenic diseases should be the simplest models for asking to what extent it is possible to predict phenotypes from genotypes. The commonest diseases caused by a single gene (monogenic diseases) in humans are the genetic disorders of haemoglobin, and these were the first to be explored at the molecular level. This article briefly outlines the progress that has been made in relating the molecular pathology of such diseases to their clinical diversity and describes the same problem for other families of monogenic disorders. Finally, I will summarise the lessons that have been learnt from studies of these conditions and what they illustrate about the kinds of difficulties that are likely to be encountered with the move towards the analysis of common multigenic disorders.

	Inherited disorders of haemoglobin

Top Inherited disorders of... The  thalassaemias Lessons for the further... Further reading

The inherited disorders of haemoglobin are by far the commonest monogenic diseases; it is estimated that about 7% of the world's population are carriers. The disorders fall into two groups: the structural variants of haemoglobin and the thalassaemias.

The structure of haemoglobin changes during embryonic, fetal, and adult life. Adult and fetal haemoglobins have  chains combined with  (haemoglobin A, ₂₂),  (haemoglobin A₂, ₂₂), or  chains (fetal haemoglobin, ₂₂). The inherited disorders of haemoglobin result from many different mutations involving either the  or  globin genes.

Although over 400 variants of structural haemoglobin have been identified, only three, haemoglobins S, C, and E, reach high frequencies in certain populations. The thalassaemias, on the other hand, which are classified into the  and  thalassaemias depending on which globin chain is ineffectively produced, are widely dispersed throughout the tropical world. I will focus on the  thalassaemias, because they are producing an increasingly serious public health problem throughout the Mediterranean region, the Middle East, the Indian subcontinent, and South East Asia.

	The  thalassaemias

Top Inherited disorders of... The  thalassaemias Lessons for the further... Further reading

Pathophysiology and clinical diversity
The hallmark of all the  thalassaemias is defective  globin synthesis, which leads to imbalanced globin chain production and an excess of  globin chains. The globin chains aggregate in red cell precursors and result in their abnormal maturation and premature destruction in the bone marrow. Abundant evidence shows that the severity of the  thalassaemias is related to the degree of imbalance of the globin chains. The excess of  globin chains precipitate and cause both mechanical damage to the red cell precursors and their products and also lead to oxidative destruction of their membranes. Imbalanced synthesis of the globin chains results in a variable degree of anaemia, which stimulates erythropoietin production, leading to intense proliferation and expansion of the bone marrow with resulting skeletal deformities. Because the red cells are abnormal they are destroyed in the spleen, which may become massively enlarged. Although the production of fetal haemoglobin is almost switched off by birth, in most normal adults some red cell precursors continue to produce a few  chains and hence a small amount of fetal haemoglobin is produced. In the face of imbalanced synthesis of the globin chain in  thalassaemia these cells come under intense selection because part of the excess of  chains are bound to  chains to produce fetal haemoglobin, thus reducing the magnitude of precipitation of the  chains. Hence in all the severe forms of  thalassaemia there is a relatively high level of fetal haemoglobin in the red cells but never enough to compensate for the overall deficit of  chains.

Phenotypic heterogeneity of  thalassaemia Homozygous or compound heterozygous states thalassaemia major; profound anaemia requiring lifelong blood transfusion thalassaemia intermedia; moderate to mild anaemia (not dependent on transfusion) Heterozygous states thalassaemia trait; mild anaemia `Silent'  thalassaemia; phenotypically normal Dominant  thalassaemia; moderate to severe anaemia

Diverse clinical phenotypes
Progress in our understanding of the clinical diversity of  thalassaemia has resulted largely from an appreciation of its pathophysiology. As mentioned, the basic defect in this disease is an inability to make  globin chains, which results in an excess of  chains that precipitate and damage the red cell precursors and their progeny. Therefore anything that tends to reduce the excess of  chains ought to ameliorate the disease, and this is indeed the case. Perhaps the most surprising outcome of this work is that although heterogeneity of the mutations at the  globin locus that underlie the  thalassaemias account for some of its clinical variability, a great deal cannot be explained in this way, and it is now clear that several other gene loci are involved.

Variable severity the  thalassaemia alleles
Over 180 different mutations have been identified in the  globin genes of patients with  thalassaemia. With the exception of a few deletions, the bulk is made up of single base changes or loss of one or two bases, all of which interfere with gene action and usually cause a drastic reduction in the output of  chains. Some of the mutations, however, involve regions of DNA (promotors) close to the  globin genes that are involved in their regulation or cause more subtle defects of gene expression during the stage when the primary product of the  globin genes is processed. Some of these mutations cause only a mild reduction in the level of  globin production. These observations account for part of the clinical diversity of  thalassaemia. Patients may be homozygous or compound heterozygous for severe mutations, in which case they have the clinical picture of thalassaemia major, or they may be similarly affected with milder mutations, which results in the intermediate forms of the disease. To complicate matters further some patients inherit a severe mutation from one parent and a mild mutation from the other, giving rise to a wide spectrum of clinical phenotypes. The silent  thalassaemias result from particularly mild mutations whereas the dominant  thalassaemias, which cause severe disease in heterozygotes, result from a particular class of mutations at one end of the  globin gene.

(Credit: JOHN BAVOSI/SCIENCE PHOTO LIBRARY) View larger version (83K): [in this window] [in a new window]   In thalassaemia, affected erythrocytes are variously shaped and fragile

Primary genetic modifiers
The excess of  chains that are produced in response to defective  chain synthesis may be modified by genetic heterogeneity at at least two other loci. In many populations in which  thalassaemia is common,  thalassaemia (a genetic defect in the production of  chains) also occurs at a high frequency. Remarkably, homozygotes or compound heterozygotes for  thalassaemia who also inherit  thalassaemia tend to have a much milder illness because of the lower concentration of excess  globin chains. Because, as with the  thalassaemias, many different mutations of varying severity underlie the  thalassaemias, this interaction alone provides the basis for considerable clinical diversity.

Secondary modifiers
As well as the effect of variability at the  and  chain loci, it is now apparent that the complications of  thalassaemia may be genetically modified by variability at many different loci. For example, there is the potential for variability at at least three different loci, which can modify the severity of the bone disease that is particularly common in patients with severe  thalassaemia. Similarly, loci have been identified that modify the rate of iron loading or the level of bilirubin in response to haemolysis and ineffective erythropoiesis, and, incidentally, the frequency of gallstone formation. There are several other examples of secondary modifiers of this type.

Phenotypic variability due to co-evolution
There is increasing evidence that the high frequency of the thalassaemias reflects heterozygote advantage against Plasmodium falciparum malaria. That every population has a different set of  thalassaemia mutations suggests that this selective force is fairly recent, otherwise the same mutations would appear throughout the tropical world. But genetic protection against P falciparum malaria is not restricted to the haemoglobin disorders. Rather, during the relatively short period (at least in evolutionary terms) that we have been exposed to this parasite many other genetic systems have been modified, including red cell enzymes and membranes, but, more importantly, the immune system and cytokines and other effectors that are involved in response to infection. These polymorphisms also vary widely among different races, again reflecting recent selection by malaria. Hence children with  thalassaemia who come from different parts of the world may have totally different responses to infection.

Ecological and ethological factors
The study of the role of the environment in modifying monogenic disease has been neglected. Increasing evidence from analyses of patients with the same mutations who live in different countries shows that environmental factors may be extremely important in determining the course of their illness. Apart from obvious factors such as socioeconomic status, availability of medical care, state of nutrition, and exposure to infection, it is apparent that more subtle effects, including climatic, may be of considerable importance.

	Lessons for the further exploration of genetic disease

Top Inherited disorders of... The  thalassaemias Lessons for the further... Further reading

Recent studies of the reasons for the clinical diversity of the  thalassaemias suggest that they reflect layer upon layer of genetic complexity, with a strong environmental component (figure). As well as remarkable heterogeneity of the primary mutations at the  globin locus, there are at least two major modifying loci, and the complications of the disease may also be fine tuned by variability at loci that have nothing to do with haemoglobin production. Each of these modifying loci may themselves show considerable heterogeneity, and the frequency of different alleles may vary widely in particular populations. The number of potential combinations, and hence phenotypes, is extremely large. What at first sight seemed to be a relatively simple monogenic disorder is, in effect, an extremely complex syndrome in which many different genes are involved together with equally numerous ill understood effects of the environment.

View larger version (37K): [in this window] [in a new window]   Factors modifying phenotypes of  thalassaemia

All monogenic diseases show considerable clinical variability, and although the defective genes have been identified and the mutations related to the phenotype in some cases, it is clear that wherever adequate studies have been done there is clinical variability among patients with the same genetic defect. No doubt the kind of modifiers that have been discovered for the thalassaemias will be identified for these other diseases. In one particular casemutations that involve transcription factors, which may be involved in the regulation of many different genes, each with their own modifierswe would expect to see widely differing phenotypes, and this is the case.

Where does this story of remarkable genetic complexity leave us when we come to consider some of the common disorders of Western society? In many cases these conditions do not show a high level of heritability. For example, concordance rates in twin studies for insulin dependent diabetes have ranged from 0.2 to 0.6 and for coronary artery disease in much the same range. This shows that these diseases, which are not inherited in a Mendelian fashion anyway, are probably the result of varying susceptibility to a wide range of environmental factors mediated by many different genes. Since each of these genes will themselves have their own modifiers, just as occurs in thalassaemia, it is clear that when we try to dissect the major loci involved in susceptibility to these diseases we are entering into another order of complexity. The situation will not be much easier in the specialty of cancer, where it is becoming apparent that there are multiple routes through oncogene mutations to many of the common cancers. The application of recently developed microchip and gene expression array technology suggests that there may be some overall pattern to the activation of different genes in the same type of cancer, and it is beginning to look as if therapy will have to be tailor made for almost every individual cancer.

These observations suggest that progress towards the clinical application of our increasing knowledge of the human genome may be slow. At the moment we cannot predict for certain the clinical course of any simple monogenic disease. The idea that we may be able to predict the occurrence of a heart attack or the onset of diabetes from examining a child's genotype at birth is even further away. Even for the monogenic diseases we still do not know what is just "noise" in the system and what is clinically important. Clearly, relating genotype to phenotype will be one of the great challenges for genetic medicine over the next century.

	Further reading

Top Inherited disorders of... The  thalassaemias Lessons for the further... Further reading

Summers KM. Relationship between genotype and phenotype in monogenic diseases: relevance to polygenic diseases. Hum Mutat 1996;7:283-93.

Todd JA. From genome to aetiology in a multifactorial disease, type 1 diabetes. BioEssays 1999;21:164-74.

Weatherall D. From genotype to phenotype: genetics and medical practice in the new millennium. Phil Trans R Soc Lond B 1999;354:1995-2010.

Weatherall DJ. Harvey lectures. The phenotypic diversity of monogenic disease: lessons from the thalassaemias. 2001 Series 94, 1-20, Wiley-Liss, Inc, New York.

Weatherall DJ, Clegg JB. The thalassaemia syndromes. 4th ed. Oxford: Blackwell Science (in press.)

Wolf U. Identical mutations and phenotypic variation. Hum Genet 1997;100:305-21.

	Acknowledgments

This is an edited version of a presentation at the Millennium Festival of Medicine in London, 6-10 November 2000.

	Footnotes

Competing interests: None declared.