Mannose-binding lectin gene sequence data in Kelantan population

被引:0
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作者
Zahidin, Muhamad Aidil [1 ]
Mohd Noor, Noor Haslina [1 ,2 ]
Johan, Muhammad Farid [1 ]
Abdullah, Abu Dzarr [3 ]
Zulkafli, Zefarina [1 ,2 ]
Edinur, Hisham Atan [4 ]
机构
[1] Univ Sains Malaysia, Sch Med Sci, Dept Haematol, Hlth Campus, Kubang Kerian 16150, Kelantan, Malaysia
[2] Hosp Univ Sains Malaysia, Transfus Med Unit, Kubang Kerian 16150, Kelantan, Malaysia
[3] Univ Sains Malaysia, Sch Med Sci, Dept Internal Med, Hlth Campus, Kubang Kerian 16150, Kelantan, Malaysia
[4] Univ Sains Malaysia, Sch Hlth Sci, Forens Sci Programme, Hlth Campus, Kubang Kerian 16150, Kelantan, Malaysia
关键词
POLYMORPHISMS; PROTEIN; ASSOCIATION; DISEASE; REVEALS; RISK;
D O I
10.1038/s41597-024-03274-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human mannose-binding lectin (MBL) gene encodes a polymorphic protein that plays a crucial role in the innate immune response. Human MBL deficiency is associated with immunodeficiencies, and its variants have been linked to autoimmune and infectious diseases. Despite this significance, gene studies concerning MBL sequencing are uncommon in Malaysia. Therefore, we aimed to preliminary described the human MBL sequencing dataset based on the Kelantan population. Blood samples were collected from 30 unrelated individuals and underwent DNA extraction, genotyping, and sequencing. The sequencing data generated 886 bp, which were deposited in GenBank (ON619541-ON619546). Allelic variants were identified and translated into six MBL haplotypes: HYPA, HYPB, LYPB, LXPB, HXPA, and LXPA. An evolutionary tree was constructed using the haplotype sequences. These findings contribute to the expansion of MBL information within the country, providing a valuable baseline for future research exploring the association between the gene and targeted diseases.
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页数:6
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