Alpha-globin gene cluster haplotypes and D1S80, D17S5, and TPO VNTR polymorphisms among four ethnic populations from lower northeastern Thailand
Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α + -thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplo...
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Published in | Scientific reports Vol. 15; no. 1; pp. 7851 - 12 |
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Main Authors | , , , , , , , |
Format | Journal Article |
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06.03.2025
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Abstract | Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α
+
-thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplotype analysis, 110 subjects with normal α-globin and 232 subjects with α
+
-thalassemia were selected to analyze six polymorphic sites using the PCR-RFLP technique. For VNTR loci analysis, 447 subjects were examined for D1S80, D17S5, and TPO allele frequencies using a PCR-based method. The results of this study revealed that the most frequent haplotypes found in Laos, including (framework 1; + M - + − 0) linked to (-α
3.7
) and (framework 3; - S - + + -) related to (α
CS
α) were different from those found in Khmer and Kui [(framework 2; + S - + − 0) linked to (-α
3.7
) and (framework 1; + M - + + -) related to (α
CS
α)]. For the (α
PS
α) gene, the haplotype (+ S - + - -) of framework 2 was found in all ethnic groups, and the haplotype (- M - + + -) of framework 1 in the Yer only. The distribution of allele frequencies for the D1S80, D17S5, and TPO VNTR loci showed extensive genetic variation in the ethnic population studied. The number of alleles is higher than that of the previously reported populations. Based on D17S5 analysis, the phylogenetic tree suggested that Khmer and Kui ethnic groups had a close relationship but were distant from Laos. In addition, ethnic relationships were observed in the Yer and Kui populations. In contrast, consistent results were not obtained based on D1S80 and TPO analysis. The findings indicate genetic variation in these ethnic populations, but the conclusion remains tentative. However, this study provides useful information to better understand genetic origins and ethnic relationships in the region. |
---|---|
AbstractList | Abstract Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α+-thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplotype analysis, 110 subjects with normal α-globin and 232 subjects with α+-thalassemia were selected to analyze six polymorphic sites using the PCR-RFLP technique. For VNTR loci analysis, 447 subjects were examined for D1S80, D17S5, and TPO allele frequencies using a PCR-based method. The results of this study revealed that the most frequent haplotypes found in Laos, including (framework 1; + M - + − 0) linked to (-α3.7) and (framework 3; - S - + + -) related to (αCSα) were different from those found in Khmer and Kui [(framework 2; + S - + − 0) linked to (-α3.7) and (framework 1; + M - + + -) related to (αCSα)]. For the (αPSα) gene, the haplotype (+ S - + - -) of framework 2 was found in all ethnic groups, and the haplotype (- M - + + -) of framework 1 in the Yer only. The distribution of allele frequencies for the D1S80, D17S5, and TPO VNTR loci showed extensive genetic variation in the ethnic population studied. The number of alleles is higher than that of the previously reported populations. Based on D17S5 analysis, the phylogenetic tree suggested that Khmer and Kui ethnic groups had a close relationship but were distant from Laos. In addition, ethnic relationships were observed in the Yer and Kui populations. In contrast, consistent results were not obtained based on D1S80 and TPO analysis. The findings indicate genetic variation in these ethnic populations, but the conclusion remains tentative. However, this study provides useful information to better understand genetic origins and ethnic relationships in the region. Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α + -thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplotype analysis, 110 subjects with normal α-globin and 232 subjects with α + -thalassemia were selected to analyze six polymorphic sites using the PCR-RFLP technique. For VNTR loci analysis, 447 subjects were examined for D1S80, D17S5, and TPO allele frequencies using a PCR-based method. The results of this study revealed that the most frequent haplotypes found in Laos, including (framework 1; + M - + − 0) linked to (-α 3.7 ) and (framework 3; - S - + + -) related to (α CS α) were different from those found in Khmer and Kui [(framework 2; + S - + − 0) linked to (-α 3.7 ) and (framework 1; + M - + + -) related to (α CS α)]. For the (α PS α) gene, the haplotype (+ S - + - -) of framework 2 was found in all ethnic groups, and the haplotype (- M - + + -) of framework 1 in the Yer only. The distribution of allele frequencies for the D1S80, D17S5, and TPO VNTR loci showed extensive genetic variation in the ethnic population studied. The number of alleles is higher than that of the previously reported populations. Based on D17S5 analysis, the phylogenetic tree suggested that Khmer and Kui ethnic groups had a close relationship but were distant from Laos. In addition, ethnic relationships were observed in the Yer and Kui populations. In contrast, consistent results were not obtained based on D1S80 and TPO analysis. The findings indicate genetic variation in these ethnic populations, but the conclusion remains tentative. However, this study provides useful information to better understand genetic origins and ethnic relationships in the region. Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α+-thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplotype analysis, 110 subjects with normal α-globin and 232 subjects with α+-thalassemia were selected to analyze six polymorphic sites using the PCR-RFLP technique. For VNTR loci analysis, 447 subjects were examined for D1S80, D17S5, and TPO allele frequencies using a PCR-based method. The results of this study revealed that the most frequent haplotypes found in Laos, including (framework 1; + M - + − 0) linked to (-α3.7) and (framework 3; - S - + + -) related to (αCSα) were different from those found in Khmer and Kui [(framework 2; + S - + − 0) linked to (-α3.7) and (framework 1; + M - + + -) related to (αCSα)]. For the (αPSα) gene, the haplotype (+ S - + - -) of framework 2 was found in all ethnic groups, and the haplotype (- M - + + -) of framework 1 in the Yer only. The distribution of allele frequencies for the D1S80, D17S5, and TPO VNTR loci showed extensive genetic variation in the ethnic population studied. The number of alleles is higher than that of the previously reported populations. Based on D17S5 analysis, the phylogenetic tree suggested that Khmer and Kui ethnic groups had a close relationship but were distant from Laos. In addition, ethnic relationships were observed in the Yer and Kui populations. In contrast, consistent results were not obtained based on D1S80 and TPO analysis. The findings indicate genetic variation in these ethnic populations, but the conclusion remains tentative. However, this study provides useful information to better understand genetic origins and ethnic relationships in the region. Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α -thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplotype analysis, 110 subjects with normal α-globin and 232 subjects with α -thalassemia were selected to analyze six polymorphic sites using the PCR-RFLP technique. For VNTR loci analysis, 447 subjects were examined for D1S80, D17S5, and TPO allele frequencies using a PCR-based method. The results of this study revealed that the most frequent haplotypes found in Laos, including (framework 1; + M - + - 0) linked to (-α ) and (framework 3; - S - + + -) related to (α α) were different from those found in Khmer and Kui [(framework 2; + S - + - 0) linked to (-α ) and (framework 1; + M - + + -) related to (α α)]. For the (α α) gene, the haplotype (+ S - + - -) of framework 2 was found in all ethnic groups, and the haplotype (- M - + + -) of framework 1 in the Yer only. The distribution of allele frequencies for the D1S80, D17S5, and TPO VNTR loci showed extensive genetic variation in the ethnic population studied. The number of alleles is higher than that of the previously reported populations. Based on D17S5 analysis, the phylogenetic tree suggested that Khmer and Kui ethnic groups had a close relationship but were distant from Laos. In addition, ethnic relationships were observed in the Yer and Kui populations. In contrast, consistent results were not obtained based on D1S80 and TPO analysis. The findings indicate genetic variation in these ethnic populations, but the conclusion remains tentative. However, this study provides useful information to better understand genetic origins and ethnic relationships in the region. Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α+-thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplotype analysis, 110 subjects with normal α-globin and 232 subjects with α+-thalassemia were selected to analyze six polymorphic sites using the PCR-RFLP technique. For VNTR loci analysis, 447 subjects were examined for D1S80, D17S5, and TPO allele frequencies using a PCR-based method. The results of this study revealed that the most frequent haplotypes found in Laos, including (framework 1; + M - + - 0) linked to (-α3.7) and (framework 3; - S - + + -) related to (αCSα) were different from those found in Khmer and Kui [(framework 2; + S - + - 0) linked to (-α3.7) and (framework 1; + M - + + -) related to (αCSα)]. For the (αPSα) gene, the haplotype (+ S - + - -) of framework 2 was found in all ethnic groups, and the haplotype (- M - + + -) of framework 1 in the Yer only. The distribution of allele frequencies for the D1S80, D17S5, and TPO VNTR loci showed extensive genetic variation in the ethnic population studied. The number of alleles is higher than that of the previously reported populations. Based on D17S5 analysis, the phylogenetic tree suggested that Khmer and Kui ethnic groups had a close relationship but were distant from Laos. In addition, ethnic relationships were observed in the Yer and Kui populations. In contrast, consistent results were not obtained based on D1S80 and TPO analysis. The findings indicate genetic variation in these ethnic populations, but the conclusion remains tentative. However, this study provides useful information to better understand genetic origins and ethnic relationships in the region.Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α+-thalassemia, but the genetic background remains poorly understood. This study examined genetic variation at the α-globin gene cluster and three VNTR loci (D1S80, D17S5, and TPO) in these ethnic populations. For α-globin haplotype analysis, 110 subjects with normal α-globin and 232 subjects with α+-thalassemia were selected to analyze six polymorphic sites using the PCR-RFLP technique. For VNTR loci analysis, 447 subjects were examined for D1S80, D17S5, and TPO allele frequencies using a PCR-based method. The results of this study revealed that the most frequent haplotypes found in Laos, including (framework 1; + M - + - 0) linked to (-α3.7) and (framework 3; - S - + + -) related to (αCSα) were different from those found in Khmer and Kui [(framework 2; + S - + - 0) linked to (-α3.7) and (framework 1; + M - + + -) related to (αCSα)]. For the (αPSα) gene, the haplotype (+ S - + - -) of framework 2 was found in all ethnic groups, and the haplotype (- M - + + -) of framework 1 in the Yer only. The distribution of allele frequencies for the D1S80, D17S5, and TPO VNTR loci showed extensive genetic variation in the ethnic population studied. The number of alleles is higher than that of the previously reported populations. Based on D17S5 analysis, the phylogenetic tree suggested that Khmer and Kui ethnic groups had a close relationship but were distant from Laos. In addition, ethnic relationships were observed in the Yer and Kui populations. In contrast, consistent results were not obtained based on D1S80 and TPO analysis. The findings indicate genetic variation in these ethnic populations, but the conclusion remains tentative. However, this study provides useful information to better understand genetic origins and ethnic relationships in the region. |
ArticleNumber | 7851 |
Author | Jomoui, Wittaya Singsanan, Sanita Fucharoen, Supan Karnpean, Rossarin Chamnanphon, Monpat Thongrung, Ruttiya Saenwang, Phairo Pansuwan, Anupong |
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Snippet | Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α
+
-thalassemia, but the genetic background remains poorly understood. This study... Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α -thalassemia, but the genetic background remains poorly understood. This study examined... Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α+-thalassemia, but the genetic background remains poorly understood. This study examined... Abstract Laos, Khmer, Kui, and Yer ethnic populations had a high prevalence of α+-thalassemia, but the genetic background remains poorly understood. This study... |
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SubjectTerms | 631/208 631/337 692/4017 Adult Alleles alpha-Globins - genetics alpha-Thalassemia - ethnology alpha-Thalassemia - genetics Blood diseases Ethnic population Ethnicity - genetics Female Gene Frequency Genetic diversity Genetic variation Haplotypes Humanities and Social Sciences Humans Male Minisatellite Repeats - genetics Minority & ethnic groups multidisciplinary Multigene Family Polymorphism, Genetic Population genetics Population studies Restriction fragment length polymorphism Science Science (multidisciplinary) Thailand Thalassemia VNTR α-globin gene haplotype |
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Title | Alpha-globin gene cluster haplotypes and D1S80, D17S5, and TPO VNTR polymorphisms among four ethnic populations from lower northeastern Thailand |
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