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FQ-RT-PCR法检测脐带血中β与γ珠蛋白mRNA的水平

MEASUREMENT OF β-AND γ-mRNA LEVELS IN THE UMBILICAL CORD BLOOD BY FLUORESCENCE QUANTITATIVE RT-PCR
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摘要 目的 :探讨新生儿脐带血中 β与 γ珠蛋白 m RNA水平及其意义。方法 :用实时荧光定量逆转录—聚合酶链反应技术检测 2 3例新生儿脐带血和 2 5例正常对照组外周血中 β与 γ珠蛋白 m RNA水平。结果 :脐带血中 γ/ (β+γ) m RNA比值 [(4 4 .0 8±2 2 .4 1 ) % ]明显高于正常对照组 [(1 .5 5± 4 .1 4 ) % ](P <0 .0 0 1 )。脐带血中胎儿血红蛋白 (Hb F)比值 [(5 8.1 1± 7.1 9) % ]也明显高于正常对照组 [(0 .6 3± 0 .32 ) % ](P <0 .0 0 1 )。结论 :脐带血中 γ/ (β+γ) m RNA及 Hb F水平增高 ,可能说明出生时 γ珠蛋白仍未完全关闭 。 Objective:To investigate the β and γ mRNA levels in the umbilical cord blood Methods:We measured the β and γ mRNA levels from red cells of 23 newborn umbilical cord blood and 25 normal controls by the fluorescence quantitative RT PCR Result:The mean γ/(β+γ) ratio in the newborn umbilical cord blood[(44 08±22 41)%] was higher than that of normal controls (P<0 001) The mean HbF ratio[(58 11±7 19)%] was significantly higher than that of normal controls [(0 63±0 32)%] (P<0 001).Conclusion:The mean γ/(β+γ) ratio and HbF rate was significantly higher than that of normal controls.It probably indicates that γ hemoglobin still has partial expression when being born.
出处 《广西医科大学学报》 CAS 2003年第3期333-334,共2页 Journal of Guangxi Medical University
基金 广西自然科学基金青年基金资助 ( No.973 2 0 0 6)
关键词 脐带血 Γ珠蛋白 MRNA Β珠蛋白 实时荧光定量逆转录-聚合酶链反应 Umbilical cord blood hemoglobin mRNA fluorescence quantitative RT PCR
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  • 1唐智宁 梁徐 等.检验ξ珠蛋白肽链诊断α地中海贫血[J].中华血液学杂志,1988,9:687-688.
  • 2Chomczynski P,Sacchi N. Single-step method of RNA isolation by acid guanidinum thiocyanate-phenol-chloroform extraction. Anal Blochem, 1987,54:1071
  • 3Karlsson S,Nienhuis AN. Developmental regulation of human globin genes. Ann Res Biochem, 1985,54:1071.
  • 4Noguera NI,Detatsio G, PEREZ SM,et al. Hematologic study of newborn umbilical Cord blood. Medicina-B-Aires, 1999,59 : 446.
  • 5Peri KG,Gagnon C,Bard H ,et al. Quantitative correlation between globin mRNA and synthesis of fetal and adult hemoglobins during hemoglobin switchover in the perinatal period. Pediatr Res, 1998,43 : 504.

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