Che Ghazali Norul Hajar, Zulkafli Zefarina, Nor Suhaila Md Riffin, Tuan Hulwani Tuan Mohammad, Mohd Nazri Hassan, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Mohd Yusmaidie Aziz, Abd Rashid Nur Haslindawaty, Geoffrey Keith Chambers, Hisham Atan Edinur
{"title":"马来西亚半岛的人类白细胞抗原-G 基因多态性:初步报告。","authors":"Che Ghazali Norul Hajar, Zulkafli Zefarina, Nor Suhaila Md Riffin, Tuan Hulwani Tuan Mohammad, Mohd Nazri Hassan, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Mohd Yusmaidie Aziz, Abd Rashid Nur Haslindawaty, Geoffrey Keith Chambers, Hisham Atan Edinur","doi":"10.1089/gtmb.2023.0492","DOIUrl":null,"url":null,"abstract":"<p><p><b><i>Introduction:</i></b> Expression of the nonclassical human leukocyte antigen (<i>HLA</i>)<i>-G</i> gene is upregulated in placenta during pregnancy. In other cells, HLA-G is upregulated during parasitic infections and allergic reactions. Polymorphism at the <i>HLA-G</i> gene locus has been reported for many populations, but so far not for any ethnic groups in Malaysia. In this survey, we screened for genetic variation in <i>HLA-G</i> genes from representative Malay, Chinese, and Indian individuals living in Peninsular Malaysia. <b><i>Materials and Methods:</i></b> Blood samples were obtained with informed consent, and ethnicity classes were assigned based on self-declared pedigree information. Exons 2, 3, and 4 of the <i>HLA-G</i> gene were amplified by polymerase chain reaction and subjected to Sanger sequencing. <b><i>Results:</i></b> The most common genotype in Malays and Indians was found to be <i>HLA-G*01:01:01:01/01:01:01:01</i> with frequencies of 0.206 and 0.167, respectively, whereas the <i>HLA-G*01:01:03:01/01:01:01:01</i> genotype was the one most frequently observed in Chinese (0.221). Based on this study, <i>HLA-G*01:01:01:01</i> (0.427-0.448) is the most frequent <i>HLA-G</i> allele in the all three ethnic groups. In contrast, <i>HLA-G*01:01:02:01</i> (0.186) was observed as the second most frequent <i>HLA-G</i> allele in Malays and <i>HLA-G*01:04:01</i> in Chinese and Indians, (0.188-0.198, respectively). Several minor <i>HLA-G</i> alleles were detected at low frequency in Malays, Chinese, or Indians (<i>HLA-G*01:01:05</i>, <i>01:01:09</i>, <i>01:04:02</i>, and <i>01:04:03</i>). These have only rarely, if ever, been reported in other population groups. Subsequent statistical analysis including using principal coordinate data mapping showed the Malays, Chinese, and Indians are distinct but quite closely related to one another as compared with other population groups from across Europe and Africa. <b><i>Conclusion:</i></b> The HLA-G population data collected in this study showed that the ancestrally unrelated Malays, Chinese, and Indians are genetically distinct. This new database provides a foundation for further studies to capture <i>HLA-G</i> allelic diversity in uncharacterized populations of Malaysia and for future attempts to identify their roles in disease resistance and susceptibility.</p>","PeriodicalId":12603,"journal":{"name":"Genetic testing and molecular biomarkers","volume":" ","pages":"393-401"},"PeriodicalIF":1.1000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Human Leukocyte Antigen-G Gene Polymorphism in Peninsular Malaysia: A Preliminary Report.\",\"authors\":\"Che Ghazali Norul Hajar, Zulkafli Zefarina, Nor Suhaila Md Riffin, Tuan Hulwani Tuan Mohammad, Mohd Nazri Hassan, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Mohd Yusmaidie Aziz, Abd Rashid Nur Haslindawaty, Geoffrey Keith Chambers, Hisham Atan Edinur\",\"doi\":\"10.1089/gtmb.2023.0492\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b><i>Introduction:</i></b> Expression of the nonclassical human leukocyte antigen (<i>HLA</i>)<i>-G</i> gene is upregulated in placenta during pregnancy. In other cells, HLA-G is upregulated during parasitic infections and allergic reactions. Polymorphism at the <i>HLA-G</i> gene locus has been reported for many populations, but so far not for any ethnic groups in Malaysia. In this survey, we screened for genetic variation in <i>HLA-G</i> genes from representative Malay, Chinese, and Indian individuals living in Peninsular Malaysia. <b><i>Materials and Methods:</i></b> Blood samples were obtained with informed consent, and ethnicity classes were assigned based on self-declared pedigree information. Exons 2, 3, and 4 of the <i>HLA-G</i> gene were amplified by polymerase chain reaction and subjected to Sanger sequencing. <b><i>Results:</i></b> The most common genotype in Malays and Indians was found to be <i>HLA-G*01:01:01:01/01:01:01:01</i> with frequencies of 0.206 and 0.167, respectively, whereas the <i>HLA-G*01:01:03:01/01:01:01:01</i> genotype was the one most frequently observed in Chinese (0.221). Based on this study, <i>HLA-G*01:01:01:01</i> (0.427-0.448) is the most frequent <i>HLA-G</i> allele in the all three ethnic groups. In contrast, <i>HLA-G*01:01:02:01</i> (0.186) was observed as the second most frequent <i>HLA-G</i> allele in Malays and <i>HLA-G*01:04:01</i> in Chinese and Indians, (0.188-0.198, respectively). Several minor <i>HLA-G</i> alleles were detected at low frequency in Malays, Chinese, or Indians (<i>HLA-G*01:01:05</i>, <i>01:01:09</i>, <i>01:04:02</i>, and <i>01:04:03</i>). These have only rarely, if ever, been reported in other population groups. Subsequent statistical analysis including using principal coordinate data mapping showed the Malays, Chinese, and Indians are distinct but quite closely related to one another as compared with other population groups from across Europe and Africa. <b><i>Conclusion:</i></b> The HLA-G population data collected in this study showed that the ancestrally unrelated Malays, Chinese, and Indians are genetically distinct. This new database provides a foundation for further studies to capture <i>HLA-G</i> allelic diversity in uncharacterized populations of Malaysia and for future attempts to identify their roles in disease resistance and susceptibility.</p>\",\"PeriodicalId\":12603,\"journal\":{\"name\":\"Genetic testing and molecular biomarkers\",\"volume\":\" \",\"pages\":\"393-401\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genetic testing and molecular biomarkers\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1089/gtmb.2023.0492\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/9/16 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genetic testing and molecular biomarkers","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1089/gtmb.2023.0492","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/16 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Human Leukocyte Antigen-G Gene Polymorphism in Peninsular Malaysia: A Preliminary Report.
Introduction: Expression of the nonclassical human leukocyte antigen (HLA)-G gene is upregulated in placenta during pregnancy. In other cells, HLA-G is upregulated during parasitic infections and allergic reactions. Polymorphism at the HLA-G gene locus has been reported for many populations, but so far not for any ethnic groups in Malaysia. In this survey, we screened for genetic variation in HLA-G genes from representative Malay, Chinese, and Indian individuals living in Peninsular Malaysia. Materials and Methods: Blood samples were obtained with informed consent, and ethnicity classes were assigned based on self-declared pedigree information. Exons 2, 3, and 4 of the HLA-G gene were amplified by polymerase chain reaction and subjected to Sanger sequencing. Results: The most common genotype in Malays and Indians was found to be HLA-G*01:01:01:01/01:01:01:01 with frequencies of 0.206 and 0.167, respectively, whereas the HLA-G*01:01:03:01/01:01:01:01 genotype was the one most frequently observed in Chinese (0.221). Based on this study, HLA-G*01:01:01:01 (0.427-0.448) is the most frequent HLA-G allele in the all three ethnic groups. In contrast, HLA-G*01:01:02:01 (0.186) was observed as the second most frequent HLA-G allele in Malays and HLA-G*01:04:01 in Chinese and Indians, (0.188-0.198, respectively). Several minor HLA-G alleles were detected at low frequency in Malays, Chinese, or Indians (HLA-G*01:01:05, 01:01:09, 01:04:02, and 01:04:03). These have only rarely, if ever, been reported in other population groups. Subsequent statistical analysis including using principal coordinate data mapping showed the Malays, Chinese, and Indians are distinct but quite closely related to one another as compared with other population groups from across Europe and Africa. Conclusion: The HLA-G population data collected in this study showed that the ancestrally unrelated Malays, Chinese, and Indians are genetically distinct. This new database provides a foundation for further studies to capture HLA-G allelic diversity in uncharacterized populations of Malaysia and for future attempts to identify their roles in disease resistance and susceptibility.
期刊介绍:
Genetic Testing and Molecular Biomarkers is the leading peer-reviewed journal covering all aspects of human genetic testing including molecular biomarkers. The Journal provides a forum for the development of new technology; the application of testing to decision making in an increasingly varied set of clinical situations; ethical, legal, social, and economic aspects of genetic testing; and issues concerning effective genetic counseling. This is the definitive resource for researchers, clinicians, and scientists who develop, perform, and interpret genetic tests and their results.
Genetic Testing and Molecular Biomarkers coverage includes:
-Diagnosis across the life span-
Risk assessment-
Carrier detection in individuals, couples, and populations-
Novel methods and new instrumentation for genetic testing-
Results of molecular, biochemical, and cytogenetic testing-
Genetic counseling