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位于γ珠蛋白基因5'端的Xmn I位点(-158,C→T):与塞内加尔单倍型及γ珠蛋白表达的相关性。

The Xmn I site (-158, C----T) 5' to the G gamma gene: correlation with the Senegalese haplotype and G gamma globin expression.

作者信息

Ballas S K, Talacki C A, Adachi K, Schwartz E, Surrey S, Rappaport E

机构信息

Cardeza Foundation for Hematologic Research, Department of Medicine, Thomas Jefferson University, Philadelphia, PA 19107.

出版信息

Hemoglobin. 1991;15(5):393-405. doi: 10.3109/03630269108998859.

Abstract

There are three major African haplotypes associated with the sickle mutation: Benin (#19), Senegalese (#3), and Central African Republic (#20). Previous studies have suggested that the Xmn I site (-158 bp 5' to the G gamma gene) is associated with elevated levels of G gamma and with the Senegalese haplotype, while other investigators questioned this association. In order to clarify the issue, we have determined beta haplotypes, tested for the presence of the Xmn I site, and measured Hb F and G gamma expression levels in 143 American Black patients with sickle cell anemia. Haplotypes were determined using eight polymorphic sites in the beta-like globin gene cluster: Hinc II 5' to epsilon, Hind III in IVS-II G gamma and A gamma, Hinc II within and 3' to psi beta, Ava II in IVS-II of beta, and Hpa I and Bam HI 3' to beta. The G gamma /A gamma ratio was analyzed by high performance liquid chromatography using a C18 column. The Xmn I site was present in all 31 chromosomes with the Sengalese haplotype. Of the remaining 255 chromosomes with other haplotypes, only 2 (0.8%) had the Xmn I site present. There was significant correlation between the presence of the Xmn I site and increased G gamma /A gamma ratio in a dose-dependent manner. The Hb F level was not significantly increased in the presence of the Xmn I site. The data indicate that the Xmn I site maintains a G gamma /A gamma ratio typical of fetal life but does not necessarily cause elevation of Hb F. The latter seems to depend on factors other than the Xmn I site.

摘要

有三种主要的与镰状突变相关的非洲单倍型

贝宁型(#19)、塞内加尔型(#3)和中非共和国型(#20)。先前的研究表明,Xmn I位点(位于Gγ基因5'端-158 bp处)与Gγ水平升高以及塞内加尔单倍型相关,而其他研究者对这种关联提出了质疑。为了阐明这个问题,我们确定了β单倍型,检测了Xmn I位点的存在情况,并测量了143例美国镰状细胞贫血黑人患者的Hb F和Gγ表达水平。使用β样珠蛋白基因簇中的八个多态性位点确定单倍型:ε基因5'端的Hinc II、IVS-II Gγ和Aγ中的Hind III、ψβ内部和3'端的Hinc II、β基因IVS-II中的Ava II以及β基因3'端的Hpa I和Bam HI。使用C18柱通过高效液相色谱分析Gγ/Aγ比值。在所有31条具有塞内加尔单倍型的染色体中都存在Xmn I位点。在其余255条具有其他单倍型的染色体中,只有2条(0.8%)存在Xmn I位点。Xmn I位点的存在与Gγ/Aγ比值增加之间存在显著的剂量依赖性相关性。在存在Xmn I位点的情况下,Hb F水平没有显著升高。数据表明,Xmn I位点维持了胎儿期典型的Gγ/Aγ比值,但不一定导致Hb F升高。后者似乎取决于Xmn I位点以外的因素。

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