Nagarajan S, Brown C J, Medof M E
Institute of Pathology, Case Western Reserve University, Cleveland, OH 44106, USA.
Hum Genet. 1995 Jun;95(6):691-7. doi: 10.1007/BF00209489.
PIG-A, the gene encoding the glycoinositol phospholipid anchor synthetic element that is defective in paroxysmal nocturnal hemoglobinuria (PNH), resides on the X chromosome. In the course of analyses of PIG-A genetic alterations in PNH patients, polymerase chain reaction (PCR) amplification of reverse-transcribed RNA from affected leukocytes of a patient with diminished PIG-A mRNA expression yielded a PIG-A related sequence with 126 nucleotide substitutions and five deletions. In the present study, the origin of this product was investigated. Selective reverse transcription (RT)/PCR amplifications with primers specific for PIG-A and this variant sequence, analyses of RNA from unaffected cells, and differential endonuclease digestions showed that mRNA with this sequence is coexpressed with PIG-A mRNA in a wide range of cell types. Mapping of genomic DNA from human/rodent hybrids showed that the sequence derives from a processed gene, designated PIG-A-II, that is encoded on chromosome 12.
PIG-A基因编码糖基磷脂酰肌醇锚合成元件,该元件在阵发性夜间血红蛋白尿(PNH)中存在缺陷,它位于X染色体上。在对PNH患者的PIG-A基因改变进行分析的过程中,从一名PIG-A mRNA表达降低的患者受影响白细胞的逆转录RNA进行聚合酶链反应(PCR)扩增,得到了一个具有126个核苷酸取代和5个缺失的PIG-A相关序列。在本研究中,对该产物的起源进行了调查。用针对PIG-A和该变异序列的特异性引物进行选择性逆转录(RT)/PCR扩增、对未受影响细胞的RNA进行分析以及差异核酸内切酶消化表明,具有该序列的mRNA在多种细胞类型中与PIG-A mRNA共表达。对人/啮齿动物杂交体的基因组DNA进行定位显示,该序列来自一个加工基因,命名为PIG-A-II,它在12号染色体上编码。