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Blood, 1 October 2004, Vol. 104, No. 7, pp. 2184-2186. Prepublished online as a Blood First Edition Paper on June 17, 2004; DOI 10.1182/blood-2004-02-0527.
RED CELLS Quantitative trait locus on chromosome 8q influences the switch from fetal to adult hemoglobinFrom the Epidemiology Division, Department of Medicine, University of California, Irvine; the Department of Environmental Health, Science, and Policy, University of California, Irvine; the Department of Haematological Medicine, Guy's, King's and St Thomas' School of Medicine, London, United Kingdom; and the St Thomas' Twins Register Unit, St Thomas' Hospital, London, United Kingdom.
The switch from fetal to adult hemoglobin is incomplete; the residual fetal hemoglobin in adults is restricted to a subset of erythrocytes called F cells. F-cell levels are influenced by a sequence variant (C  T) at position -158 upstream of the  -globin gene, termed the XmnI-G polymorphism. How the G-158 C T variant influences the expression of the G-globin gene is unknown but is likely to involve the interaction of a multiprotein transcription complex. In a recent genome-wide linkage study of a large Asian Indian kindred, a genetic interaction between the XmnI-G site and a locus on chromosome 8q was reported to influence adult F-cell levels. We report the replication of linkage to chromosome 8q in a sample of European twin pairs. This result provides strong evidence that a quantitative trait locus exists on chromosome 8q that influences the developmental switch from fetal to adult hemoglobin. (Blood. 2004;104:2184-2186)
Residual amounts of fetal hemoglobin (Hb F) continue to be synthesized throughout adult life and are restricted to a subset of erythrocytes termed F cells (FCs).1 There is a good correlation between the percentages of Hb F and FCs, indicating that increased Hb F can be ascribed to the higher number of F cells produced.2 The heritability of FC levels was estimated to be 0.89 in the European population.3 Epidemiologic studies have shown FCs to be influenced by age,4 sex,5 and a DNA sequence variant (C T) at position -158 upstream of the G-globin gene, referred to as the XmnI-G polymorphism.6-8 The XmnI-G polymorphism is common in several populations; the "T" variant, which creates a cleavage site for the XmnI restriction enzyme, has been shown to be associated with increased FC levels.7 The frequency of the XmnI-G restriction site is approximately 0.33 in Europeans, and the genotype accounts for 13% to 32% of the total phenotypic variance.8 The G-158 T variant predisposes toward increased Hb F production in adult life, particularly in conditions of erythroid stress, such as  -thalassemia9-11 and sickle cell anemia.9 However, unlike rare mutations in the -globin promoter that are associated with clearly defined phenotypes of elevated Hb F levels of 10% to 35% in heterozygotes,2 the G-158 variant does not always raise Hb F levels in otherwise healthy individuals. Even within families with heterocellular hereditary persistence of fetal hemoglobin (HPFH) in which increased Hb F was associated with XmnI-G T/T or T/C genotypes, the association is not complete.12 Nearly half of the family members with these XmnI-G genotypes do not have increased Hb F levels, suggesting that the effect of the XmnI-G site is modulated by the presence of an intermediary factor(s). The most consistent change caused by the T allele at G-158 is a high proportion of G chains.
Linkage has been reported between 3 regions of the genome and adult Hb F or FC levels. Chromosome Xp22.2-p22.3 has been linked to FC levels in sickle cell disease and healthy individuals.13 A locus has been mapped to chromosome 6q23 in a large Asian Indian kindred with
A total of 319 same-sex dizygotic (DZ) twin pairs of European descent were phenotyped for FC levels and genotyped for 19 markers spanning 57 cM of chromosome 8. The twin pairs were from St Thomas's United Kingdom Adult Twin (TwinsUK) Register3,17 and were not selected for Hb F or FC levels. Details of the twin registry, the sample, and the determination of the FC levels and XmnI-G genotypes are described elsewhere.3,17 The average age was 53 years, ranging from 24 to 77 years. The average FC level of the sample was 4.04% of total erythrocytes (standard deviation, 2.87%; range, 0.53%-17.9%). FC levels were log transformed to fit the normal distribution. FC levels were adjusted to remove the effect of the XmnI-G genotype when indicated in the results. The additive effect of the T allele was estimated by linear regression. The estimated regression coefficient, , was subtracted from the FC values; 1 x for those individuals having T/C genotypes and 2 x for those individuals having T/T genotypes. This resulted in the mean FC levels being equal for each XmnI-G genotype group and a reduction in the variance of the overall trait distribution. The Marshfield chromosome 8 sex-averaged linkage map18 was used to determine the order and interval distances of the 19 markers (Figure 1). Multipoint quantitative trait linkage analysis was carried out by using the MAPMAKER/SIBS program.19 The proportion of identity-by-descent (IBD) information extracted by the markers was 0.78, ranging from 0.68 to 0.86.
Multipoint linkage analyses of the XmnI-G adjusted and unadjusted FC trait were carried out with the results shown in Figure 1. The XmnI-G adjusted FC trait showed higher multipoint logarithm of odds (lod) scores across the 56-cM interval than the unadjusted trait. The maximum lod score was 2.76 at the 16-cM position on the map; 0.5 cM was from marker D8S255. A confidence interval of one lod score unit ranges 21 cM from position 10 to 31 cM. Linkage analysis of the unadjusted FC levels showed a multipoint curve that was similar to the XmnI-G adjusted data; however, the lod score values were lower across the interval. The maximum lod score for the unadjusted data was 1.99 at the 15-cM position. The results shown in Figure 1 represent a confirmation of the earlier significant linkage reported by Garner et al16 on chromosome 8q in an independent sample from a different human population. The results meet the criteria of a confirmed linkage given by Lander and Kruglyak.20 The sample size in the present study was not large enough to test specific models of genetic interaction between the chromosome 8q QTL and the XmnI-G genotype. The higher lod scores observed for the XmnI-G-adjusted FC trait suggest that a conditional or epistatic interaction between the 2 QTLs may not be the predominant model of FC inheritance in the European sample.
The vertical bars in Figure 1 show the single-point lod scores computed under a 2-locus model in the original genomewide linkage study of the Asian Indian kindred.16 The maximum single-point lod score was 4.33 at marker D8S1833 (see Table 1 in Garner et al16). Marker D8S538 was mapped to the same location as D8S1833 and showed an lod score of 3.14. The best estimate of the location of the chromosome 8q QTL, from the current and from the original linkage studies, was within a 5-cM region between locations 15 and 20 on the map shown in Figure 1. Single-locus analysis of the chromosome 8q region showed significant linkage when the XmnI-G
The chromosome 8q QTL could be a trans-acting factor, affecting FC levels independent of the
We thank Claire Steward for help in preparation of the manuscript.
Submitted February 11, 2004; accepted May 26, 2004.
Prepublished online as Blood First Edition Paper, June 17, 2004; DOI 10.1182/blood-2004-02-0527.
Supported by grant 5 R01 HL69259-03 from the National Institutes of Health/National Heart, Lung, and Blood Institute (NIH/NHLBI) (S.L.T. and C.G.), and, in part, by a grant G0000111 from the Medical Research Council UK (S.L.T.).
The TwinsUK cohort is supported by the Wellcome Trust.
C.G. and N.S. contributed equally to this study.
The publication costs of this article were defrayed in part by page charge payment. Therefore, and solely to indicate this fact, this article is hereby marked "advertisement" in accordance with 18 U.S.C. section 1734.
Reprints: Chad Garner, Epidemiology Division, Department of Medicine, University of California Irvine, 224 Irvine Hall, Irvine, CA 92697-7550; e-mail: cgarner{at}uci.edu.
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Abstract
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