Molecular polymorphism Analysis on CD36 Deficiency among Platelet Blood Donors in Shenzhen.
10.19746/j.cnki.issn.1009-2137.2022.03.036
- Author:
Yun-Ping XU
1
;
Ze-Tao SUN
1
;
Long PENG
1
;
Shuang LIANG
1
;
Fan WU
1
;
Zhen LI
1
;
Da-Cheng LI
2
Author Information
1. Shenzhen Blood Center, Institution of Transfusion Medicine, Shenzhen 518035, Guangdong Province, China.
2. Shenzhen Blood Center, Institution of Transfusion Medicine, Shenzhen 518035, Guangdong Province, China,E-mail: lidachegn@hotmail.com.
- Publication Type:Journal Article
- Keywords:
CD36;
platelet;
polymorphism
- MeSH:
Blood Donors;
Blood Platelet Disorders/metabolism*;
Blood Platelets/metabolism*;
CD36 Antigens/metabolism*;
Female;
Genetic Diseases, Inborn;
Humans;
Male
- From:
Journal of Experimental Hematology
2022;30(3):884-889
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the molecular polymorphisms of CD36 among 58 blood donors with CD36 deficiency and compare with CD36 positive controls.
METHODS:A total of 58 donors with CD36 deficiency during a screening conducted in the laboratory from September 2019 to December 2020 were enrolled as the test group, including 39 males and 19 females, while 120 platelet donors with CD36 positive were randomly selected as the controls, including 76 males and 44 females. All of the subjects were Han nationality. The PCR-SBT method was used to detect coding region of CD36 gene, and molecular mutations were compared with those CD36 positive controls.
RESULTS:Among the 58 donors with CD36 deficiency, mutations appears in 32 individuals. The detection rate for type I was 71.43% (5/7), and type II was 51.92% (27/52), while among the 120 controls, mutations appears in 12 donors (10%). In the CD36 antigen-deficient donors, 16 variations were found, in which 329-330 del AC with the highest frequency accounted for 20.69%, followed by 1228-1239 del ATTGTGCCTATT(15.52%) and 1156 C>T(10.34%). Two variations, 198-205 del GATCTTTG and 220 C>T, led to premature termination of translation; four mutations, 329-330 del AC, 560 ins T, 1011-1049 39bp dupl and 1343-1344 ins TCTT, caused translation frame shift; 1228-1239 del ATTGTGCCTATT led to deletion of four amino acids (Ile-Val-Pro-Ile) at sites 410-413 of the peptide chain. The 1140 T>A and 1275 G>A were synonymous mutations, and the other 7 mutations resulted in the substitution of single nucleotide. The platelet expression in the donors of CD36 positive with 329-330 del AC or 1228-1239 del ATTGTGCCTATT mutation (heterozygote) was lower than those CD36 positive individuals without mutations (homozygote).
CONCLUSION:Multiple gene mutations in the CD36 coding region may cause CD36 deficiency, and the heterozygous individuals with mutations may lead to CD36 antigen reduction or deletion. Mutation is not detected in 44.83% of CD36 deficient individuals, there may be some other reasons for the CD36 antigen deficiency.
