Sanghera D K, Nestlerode C S, Ferrell R E, Kamboh M I
Department of Human Genetics, Graduate School of Public Health, 130 DeSoto Street, University of Pittsburgh, PA 15261, USA.
Hum Genet. 2001 Jul;109(1):63-72. doi: 10.1007/s004390100549.
Apolipoprotein H (apoH, protein; APOH, gene) is a 50-kDa glycoprotein that binds to negatively charged substrates, including phospholipids. ApoH is a main target antigen for the binding of antiphospholipid antibodies that are associated with thrombotic events. We have previously characterized the structural organization of the human APOH gene. Because of the significant structural homology between the human and chimpanzee genomes, we have employed oligonucleotides from the human APOH gene sequence to amplify chimpanzee DNA covering the entire transcribed region together with flanking sequence in the 5' region. As in humans, the chimpanzee APOH gene consists of eight exons and seven introns and encodes for a 326-amino-acid protein. The deduced amino acid and nucleotide sequence show 99.4% and 99.6% similarity between human and chimpanzee APOH, respectively. Using isoelectric focusing (IEF) and immunoblotting, we screened 155 chimpanzees (128 unrelated captured parents and 27 captive-born offspring) for the apoH protein polymorphism. The most common IEF pattern in chimpanzees was identical to a previously described APOH3 allele in humans. In addition, an anodally shifted pattern was observed in chimpanzees with an allele frequency of 0.168, and the corresponding allele was designated as APOH4. DNA sequencing of APOH*4 carriers revealed a missense mutation in exon 6 (A-->G) at codon 210, which replaces the amino acid lysine by glutamic acid. This mutation does not affect the binding of apoH to cardiolipin as revealed by cardiolipin/enzyme-linked immunosorbent assay (ELISA). We also evaluated the prevalence of anti-apoH antibodies in chimpanzee plasma by using human-apoH-based ELISA and the association of the Lys210Glu mutation with the occurrence of anti-apoH antibodies. The prevalence of anti-apoH antibodies in chimpanzees (64%) was found to be unusually high compared with that found in humans. However, the Lys210Glu mutation showed no association with the occurrence of anti-apoH antibodies. The prevalence of anti-apoH antibodies in chimpanzees may serve as a useful animal model for the human antiphospholipid syndrome, where these antibodies are associated with clinical manifestations.
载脂蛋白H(apoH,蛋白质;APOH,基因)是一种50千道尔顿的糖蛋白,可与包括磷脂在内的带负电荷的底物结合。ApoH是与血栓形成事件相关的抗磷脂抗体结合的主要靶抗原。我们之前已对人类APOH基因的结构组织进行了表征。由于人类和黑猩猩基因组之间存在显著的结构同源性,我们利用来自人类APOH基因序列的寡核苷酸来扩增黑猩猩DNA,其覆盖整个转录区域以及5'区域的侧翼序列。与人类一样,黑猩猩APOH基因由八个外显子和七个内含子组成,并编码一种326个氨基酸的蛋白质。推导的氨基酸和核苷酸序列显示,人类和黑猩猩APOH之间的相似性分别为99.4%和99.6%。我们使用等电聚焦(IEF)和免疫印迹法,对155只黑猩猩(128只无关的捕获亲本和27只圈养出生的后代)进行了apoH蛋白多态性筛查。黑猩猩中最常见的IEF模式与人类中先前描述的APOH3等位基因相同。此外,在黑猩猩中观察到一种向阳极移动的模式,其等位基因频率为0.168,相应的等位基因被指定为APOH4。对APOH*4携带者的DNA测序揭示了第6外显子(A→G)密码子210处的一个错义突变,该突变将氨基酸赖氨酸替换为谷氨酸。如通过心磷脂/酶联免疫吸附测定(ELISA)所揭示的,该突变不影响apoH与心磷脂的结合。我们还通过使用基于人apoH的ELISA评估了黑猩猩血浆中抗apoH抗体的流行率,以及Lys210Glu突变与抗apoH抗体发生之间的关联。发现黑猩猩中抗apoH抗体的流行率(64%)与人类相比异常高。然而,Lys21Glu突变与抗apoH抗体的发生没有关联。黑猩猩中抗apoH抗体的流行率可能作为人类抗磷脂综合征的一种有用动物模型,在该综合征中这些抗体与临床表现相关。