Chérif-Zahar B, Raynal V, D'Ambrosio A M, Cartron J P, Colin Y
Unité INSERM U76, Institut National de Transfusion Sanguine, Paris, France.
Blood. 1994 Dec 15;84(12):4354-60.
Rh blood group antigens of the D, C/c, and E/e series are carried by at least three red cell membrane polypeptides encoded by two highly related genes, RHD and RHCE. Homozygous individuals carrying the D--, Dc-, and DCw- gene complexes are characterized by a total or partial lack of expression of the RHCE-encoded antigens. Analysis of the molecular genetic basis of these rare conditions indicates that complete or partial expression defect of Cc/Ee antigens result from different alterations at the RH locus, but not from gross deletions. No rearrangement or mutation of the RHCE gene could be detected in donors homozygous for the D-- complex, suggesting that the lack of the Cc and Ee antigens might result from a reduced transcriptional activity of the RHCE gene. The Dc- and DCw- gene complexes, however, exhibited an important rearrangement of the RHCE gene. Instead of the normal RHCE gene, both variants carried a hybrid RHCE-D-CE gene in which exons 4 to 9 (Dc- complex) and 2 (or 3) to 9 (DCw- complex) of the RHCE gene, respectively, have been substituted by the equivalent region of the RHD gene. These gene conversion events provide an explanation for the well-described abnormal antigen profiles associated with the Dc- and DCw- complexes, like the increased expression of RhD, the reduced expression of RhC/c or RhCw, and the absence of RhE/e.
D、C/c和E/e系列的Rh血型抗原由两个高度相关的基因RHD和RHCE编码的至少三种红细胞膜多肽携带。携带D--、Dc-和DCw-基因复合体的纯合个体的特征是RHCE编码的抗原完全或部分缺乏表达。对这些罕见情况的分子遗传基础分析表明,Cc/Ee抗原的完全或部分表达缺陷是由RH基因座的不同改变引起的,而非大片段缺失。在D--复合体纯合的供体中未检测到RHCE基因的重排或突变,这表明Cc和Ee抗原的缺乏可能是由于RHCE基因转录活性降低所致。然而,Dc-和DCw-基因复合体表现出RHCE基因的重要重排。这两种变体均未携带正常的RHCE基因,而是携带了一个杂交的RHCE-D-CE基因,其中RHCE基因的外显子4至9(Dc-复合体)和2(或3)至9(DCw-复合体)分别被RHD基因的等效区域取代。这些基因转换事件解释了与Dc-和DCw-复合体相关的、已被充分描述的异常抗原谱,如RhD表达增加、RhC/c或RhCw表达降低以及RhE/e缺失。