Miraglia del Giudice E, Lombardi C, Francese M, Nobili B, Conte M L, Amendola G, Cutillo S, Iolascon A, Perrotta S
Dipartimento di Pediatria, Seconda Università degli Studi di Napoli, Italy.
Br J Haematol. 1998 May;101(2):251-4. doi: 10.1046/j.1365-2141.1998.00688.x.
This report represents an attempt to define the rate of beta-spectrin de novo mutations affecting mRNA accumulation in patients with hereditary spherocytosis (HS). 19 HS children with haematologically normal parents and varying degrees of spectrin deficiency were studied. 13 of the 19 cases who were heterozygous at the genomic level for polymorphisms in the beta-spectrin coding region were further studied. However, in an analysis of reverse-transcripted amplified cDNA from the regions of the polymorphisms, seven patients appeared to be homozygous, suggesting the occurrence of de novo mutational events affecting expression of one beta-spectrin allele. We conclude that in HS patients with isolated spectrin reduction and normal parents the apparently recessive pattern of inheritance may frequently be associated with de novo monoallelic expression of beta-spectrin.
本报告旨在确定影响遗传性球形红细胞增多症(HS)患者中β-血影蛋白从头突变率对mRNA积累的影响。研究了19名父母血液学正常且血影蛋白缺乏程度不同的HS儿童。对19例β-血影蛋白编码区多态性在基因组水平为杂合子的病例中的13例进行了进一步研究。然而,在对多态性区域的逆转录扩增cDNA分析中,7名患者似乎是纯合子,这表明发生了影响一个β-血影蛋白等位基因表达的从头突变事件。我们得出结论,在血影蛋白单独减少且父母正常的HS患者中,明显的隐性遗传模式可能经常与β-血影蛋白的从头单等位基因表达有关。