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一种确定人类红细胞丹图抗原的基因组杂交体的特征:丹图基因被复制并与一个δ血型糖蛋白基因缺失相关联。

Characterization of a genomic hybrid specifying the human erythrocyte antigen Dantu: Dantu gene is duplicated and linked to a delta glycophorin gene deletion.

作者信息

Huang C H, Blumenfeld O O

机构信息

Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461.

出版信息

Proc Natl Acad Sci U S A. 1988 Dec;85(24):9640-4. doi: 10.1073/pnas.85.24.9640.

Abstract

Dantu is a rare antigen of the human MNSs blood group system carried by a hybrid glycophorin on the erythrocyte membrane. To delineate its structure and relationship to alpha and delta glycophorins at the genomic level, we analyzed DNA from a three-generation family, in which both the presence of Dantu and Mi-III (another rare MNSs antigen) and the absence of delta glycophorin were seen. Three gross alterations in the gene cluster correlated with the observed phenotypes. Differential hybridization, secondary restriction analysis, and sequence-specific oligonucleotide probing established that Dantu glycophorin is encoded by a distinct hybrid gene derived from fusion of delta and alpha genes. The junction point of the Dantu gene was assigned to the region spanning codons 31-39 of delta and codons 72-79 of alpha genes. Dosage quantitation suggested that Dantu gene is duplicated and tandemly arranged. Identification of delta gene deletion disclosed the molecular basis for the absence of delta glycophorin in two Dantu and Mi-III double heterozygotes. The DNA inheritance pattern together with DNA typing of MN blood groups verified the genotypes and established that the duplicated Dantu hybrid gene is linked to alpha M gene as well as a delta gene deletion. The origin of such a haplotype in a segment of Black population would require two recombination events via either unequal homologous crossing-over or gene conversion.

摘要

丹图(Dantu)是人类MNSs血型系统中的一种稀有抗原,由红细胞膜上的一种杂合血型糖蛋白携带。为了在基因组水平上描绘其结构以及与α和δ血型糖蛋白的关系,我们分析了一个三代家族的DNA,该家族中既存在丹图和Mi-III(另一种稀有MNSs抗原),又不存在δ血型糖蛋白。基因簇中的三处重大改变与观察到的表型相关。差异杂交、二级限制性分析和序列特异性寡核苷酸探测确定,丹图血型糖蛋白由一个源自δ基因和α基因融合的独特杂合基因编码。丹图基因的连接点被定位到跨越δ基因第31 - 39密码子和α基因第72 - 79密码子的区域。剂量定量分析表明丹图基因是重复且串联排列的。δ基因缺失的鉴定揭示了两名丹图和Mi-III双杂合子中不存在δ血型糖蛋白的分子基础。DNA遗传模式以及MN血型的DNA分型验证了基因型,并确定重复的丹图杂合基因与αM基因以及一个δ基因缺失相连。在一部分黑人人群中这种单倍型的起源需要通过不等位同源交叉或基因转换发生两次重组事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df91/282823/3d88aedc28fa/pnas00303-0277-a.jpg

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