Giglioni B, Comi P, Taramelli R, Pozzoli M, Zanollo A, Ottolenghi S, Gianni A M
Eur J Biochem. 1979 Apr;95(3):527-31. doi: 10.1111/j.1432-1033.1979.tb12993.x.
A Southern Italian patient homozygous for hemoglobin Lepore disease synthesizes approximately 3% Lepore delta beta-globin chains (relative to alpha chains) in the reticulocytes. Measurement of beta-like RNA sequences by hybridization to complementary DNA specific for beta-globin demonstrates a low level (1--2% relative to alpha sequences) of these sequences in cytoplasmic RNA from reticulocytes or spleen cells, suggesting that the Lepore gene is expressed into mRNA at a lower extent than normal alpha or beta genes; the comparison with the level of beta-like sequences found in nuclear RNA (6--8%) further supports this conclusion and indicates, in addition, that Lepore RNA might be degraded at a faster rate than normal. 2--3% beta-like sequences are found in nuclear RNA in three cases of homozygous beta0-thalassemia, setting the highest possible estimate for the delta-RNA level; this figure suggests that the 'delta-promoter'-dependent Lepore delta beta gene is somehow more actively expressed than the delta gene.
一名患有血红蛋白Lepore病的纯合子意大利南部患者,其网织红细胞中合成的Leporeδβ-珠蛋白链约占α链的3%。通过与β-珠蛋白特异性互补DNA杂交来测量β样RNA序列,结果显示网织红细胞或脾细胞的细胞质RNA中这些序列的水平较低(相对于α序列为1%-2%),这表明Lepore基因转录为mRNA的程度低于正常的α或β基因;与核RNA中发现的β样序列水平(6%-8%)进行比较进一步支持了这一结论,此外还表明Lepore RNA的降解速度可能比正常RNA更快。在三例纯合子β0-地中海贫血患者的核RNA中发现了2%-3%的β样序列,这为δ-RNA水平设定了最高可能估计值;该数字表明依赖“δ启动子”的Leporeδβ基因在某种程度上比δ基因表达更活跃。