中华医学遗传学杂志
中華醫學遺傳學雜誌
중화의학유전학잡지
CHINESE JOURNAL OF MEDICAL GENETICS
2011年
5期
548-551
,共4页
洪小珍%应燕玲%许先国%马开荣%兰小飞%刘瑛%朱发明%吕杭军%严力行
洪小珍%應燕玲%許先國%馬開榮%蘭小飛%劉瑛%硃髮明%呂杭軍%嚴力行
홍소진%응연령%허선국%마개영%란소비%류영%주발명%려항군%엄역행
ABx09表型%ABO基因%抗B抗体
ABx09錶型%ABO基因%抗B抗體
ABx09표형%ABO기인%항B항체
ABx09 phenotype%ABO gene%anti-B antibody
目的 研究1例ABO亚型ABx09的分子机制.方法 应用单克隆抗体检测先证者红细胞ABO血型抗原,标准A、B、O红细胞检测先证者血清中的ABO抗体,采用聚合酶链反应(polymerase chain reaction,PCR)技术分别扩增先证者ABO基因的第1~7外显子序列,PCR产物经酶切后直接测序分析.第5~7外显子扩增产物经TOPO TA克隆到质粒载体中获得单链,对所得克隆进行ABO基因第5~7外显子双向测序分析.家系调查采集先证者父母的标本进行血型血清学实验和ABO基因第6和7外显子直接测序分析.结果 先证者红细胞有A、B抗原,同时血清中存在抗B抗体.直接测序分析发现第6外显子第261位无缺失、第297位AG,第7外显子467CT、526CG、657CT、703GA、796CA、803GC、889GA、930GA杂合,可指定为A102Bx09基因型.克隆测序得到两个等位基因A102和Bx09.与B101序列相比,Bx09第889位G→A,导致第297位谷氨酸变成赖氨酸.家系调查显示先证者Bx09等位基因从母亲遗传所得.结论 α-1,3-半乳糖基转移酶基因第889位G→A突变导致产生Bx09表型,其血清中可含有抗B抗体.
目的 研究1例ABO亞型ABx09的分子機製.方法 應用單剋隆抗體檢測先證者紅細胞ABO血型抗原,標準A、B、O紅細胞檢測先證者血清中的ABO抗體,採用聚閤酶鏈反應(polymerase chain reaction,PCR)技術分彆擴增先證者ABO基因的第1~7外顯子序列,PCR產物經酶切後直接測序分析.第5~7外顯子擴增產物經TOPO TA剋隆到質粒載體中穫得單鏈,對所得剋隆進行ABO基因第5~7外顯子雙嚮測序分析.傢繫調查採集先證者父母的標本進行血型血清學實驗和ABO基因第6和7外顯子直接測序分析.結果 先證者紅細胞有A、B抗原,同時血清中存在抗B抗體.直接測序分析髮現第6外顯子第261位無缺失、第297位AG,第7外顯子467CT、526CG、657CT、703GA、796CA、803GC、889GA、930GA雜閤,可指定為A102Bx09基因型.剋隆測序得到兩箇等位基因A102和Bx09.與B101序列相比,Bx09第889位G→A,導緻第297位穀氨痠變成賴氨痠.傢繫調查顯示先證者Bx09等位基因從母親遺傳所得.結論 α-1,3-半乳糖基轉移酶基因第889位G→A突變導緻產生Bx09錶型,其血清中可含有抗B抗體.
목적 연구1례ABO아형ABx09적분자궤제.방법 응용단극륭항체검측선증자홍세포ABO혈형항원,표준A、B、O홍세포검측선증자혈청중적ABO항체,채용취합매련반응(polymerase chain reaction,PCR)기술분별확증선증자ABO기인적제1~7외현자서렬,PCR산물경매절후직접측서분석.제5~7외현자확증산물경TOPO TA극륭도질립재체중획득단련,대소득극륭진행ABO기인제5~7외현자쌍향측서분석.가계조사채집선증자부모적표본진행혈형혈청학실험화ABO기인제6화7외현자직접측서분석.결과 선증자홍세포유A、B항원,동시혈청중존재항B항체.직접측서분석발현제6외현자제261위무결실、제297위AG,제7외현자467CT、526CG、657CT、703GA、796CA、803GC、889GA、930GA잡합,가지정위A102Bx09기인형.극륭측서득도량개등위기인A102화Bx09.여B101서렬상비,Bx09제889위G→A,도치제297위곡안산변성뢰안산.가계조사현시선증자Bx09등위기인종모친유전소득.결론 α-1,3-반유당기전이매기인제889위G→A돌변도치산생Bx09표형,기혈청중가함유항B항체.
Objective To analyze the molecular basis for an individual with ABx09 phenotype of ABO subtype.Methods The ABO group antigens on red blood cells of the proband were identified by monoclonal antibodies,and the ABO antibody in serum was detected by standard A,B,O cells.The exons 1-7 of ABO gene were amplified by polymerase chain reaction (PCR) respectively and the PCR products were sequenced directly.The amplified products for exons 5-7 were also cloned by TOPO TA cloning sequencing kit to split the two alleles apart,selected colonies were sequenced bidirectionally for exons 5-7 of the ABO gene.The samples of the proband's parents were collected,then serological test of the blood group and sequence analysis for exons 6-7 of ABO gene were preformed.Results Both A and B antigens were detected on red blood cells of the proband and there was anti-B antibody in the serum.There was no G deletion at position 261,while 297AG in exon 6,467CT,526CG,657CT,703GA,796CA,803GC,889GA and 930GA heterozygote in exon 7 were detected by direct DNA sequencing,which can be assigned for A102Bx09 genotype.After cloning and sequencing,two alleles A102 and Bx09 were obtained.The sequence of Bx09 had one nucleotide changes (G to A) at position 889 compared with that of B101,which resulted in an amino acid change of Glu to Lys at 297 position.The Bx09 in the proband was inherited from her mother by family investigation.Conclusion G→A at nt889 of α-1,3 galactosyltransferase gene can result in Bx09 phenotype,with the presence of anti-B antibody in serum.