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在祖籍为中国南方的患者中检测到3例血红蛋白G-中国变种。

Three cases of the hemoglobin G-Chinese variant detected in patients of southern Chinese origin.

作者信息

Wang Peng-Peng, Lin Min, Wu Jiao-Ren, Wang Xian-Yao, Yang Li-Ye

机构信息

Central Laboratory, Chaozhou Central Hospital, Chaozhou 521021, P.R. China.

出版信息

Mol Med Rep. 2010 May-Jun;3(3):459-61. doi: 10.3892/mmr_00000280.

Abstract

Hemoglobin (Hb) G-Chinese [α30 (B11) Glu↷Gln], also known as Hb G-Honolulu, Hb G-Hongkong or Hb G-Singapore, was first identified in a Chinese woman in Singapore, and was subsequently observed in several Chinese families. This Hb variant results from a GAG↷CAG mutation at codon 30 of the α-globin gene. The aim of the present study was to identify the Hb G-Chinese mutation in three Cantonese individuals. The presence of the Hb variant was confirmed by cellulose acetate electrophoresis. DNA analysis based on the polymerase chain reaction (PCR) and sequencing were conducted to confirm the presence of the mutation in the α-globin gene. A G↷C substitution at codon 30 of the α2-globin gene was observed. According to a previous study, the G↷C substitution in Hb G-Chinese creates a PstI restriction site; we amplified the α2-globin gene, then digested the PCR products with PstI. The results indicated that only the PCR product of Hb G-Chinese α2-globin was cut by PstI. The digestive products were 120 and 730 bp, respectively. Therefore, we determined that the three cases were of the heterozygous Hb G-Chinese variant.

摘要

血红蛋白G-中国人型[α30(B11)谷氨酸→谷氨酰胺],也被称为血红蛋白G-檀香山型、血红蛋白G-香港型或血红蛋白G-新加坡型,最初在新加坡的一名中国女性中被发现,随后在多个中国家庭中被观察到。这种血红蛋白变异体是由α-珠蛋白基因第30密码子处的GAG→CAG突变引起的。本研究的目的是在三名广东人中鉴定血红蛋白G-中国人型突变。通过醋酸纤维素电泳确认了血红蛋白变异体的存在。基于聚合酶链反应(PCR)和测序进行DNA分析,以确认α-珠蛋白基因中突变的存在。观察到α2-珠蛋白基因第30密码子处有G→C替换。根据先前的一项研究,血红蛋白G-中国人型中的G→C替换产生了一个PstI限制性酶切位点;我们扩增了α2-珠蛋白基因,然后用PstI消化PCR产物。结果表明,只有血红蛋白G-中国人型α2-珠蛋白的PCR产物被PstI切割。消化产物分别为120和730 bp。因此,我们确定这三例为血红蛋白G-中国人型变异体杂合子。

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