Day N K, L'Esperance R, Good R A, Michael A F, Hansen J A, Dupont B, Jersild C
J Exp Med. 1975 Jun 1;141(6):1464-9. doi: 10.1084/jem.141.6.1464.
Herediatary C2-deficiency has been shown to be transmitted asn an autosomal recessive characteristic. Recent evidence indicates that some genetic factors involved in the control of the complement (C) system in both man and mice are governed by genes localized within the major histocompatibility regionmthis study describes a large pedigree of the paternal family of a C2-deficient patient with systemic lupus erythematosusl It is shown that this condition is transmitted as an autosomal recessive trait, the heterozygous carriers having approximately half normal levels of C2. Furthermore, this trait was shown to be inherited in close linkage with an infrequent HL-A typw, 2,4A2. The maternal, C2-defective chromosome was shown to be transmitted by HL-AW10, W18 haplotypemthis same haplotype was described in a similar study by Fu et al. (6) to be associated with C2 deficiencymfinally, a third haplotype HL-A2,W18 carrying a defective C2 gene was demonstrated in a part of this pedigree.
遗传性C2缺陷已被证明是以常染色体隐性特征进行遗传的。最近的证据表明,人和小鼠体内参与补体(C)系统控制的一些遗传因子受位于主要组织相容性区域内的基因调控。本研究描述了一名患有系统性红斑狼疮的C2缺陷患者父系家族的一个大家系。结果表明,这种情况是以常染色体隐性性状进行遗传的,杂合子携带者的C2水平约为正常水平的一半。此外,该性状被证明与一种罕见的HL - A型别2,4A2紧密连锁遗传。母亲的C2缺陷染色体由HL - AW10、W18单倍型传递,傅等人(6)在一项类似研究中描述了相同的单倍型与C2缺陷有关。最后,在这个家系的一部分中发现了携带缺陷C2基因的第三种单倍型HL - A2,W18。