Maréchal J, Wilmotte R, Kanzaki A, Dhermy D, Garbarz M, Galand C, Tang T K, Yawata Y, Delaunay J
Laboratoire de Génétique Moléculaire Humaine, CNRS URA 1171, Institut Pasteur de Lyon, France.
Br J Haematol. 1995 Jul;90(3):553-56. doi: 10.1111/j.1365-2141.1995.tb05583.x.
Allele alpha LELY is a low-expression allele of erythroid spectrin alpha-chain. It carries mutations both in exon 40 and intron 45 and is associated with partial skipping of exon 46. Allele alpha LELY remains asymptomatic by itself. In contrast, it enhances the expression level of deleterious alpha-alleles occurring in trans, and as such has clinical importance. The aim of this study was to evaluate the incidence of allele alpha LELY in various ethnic groups, i.e. Caucasians, African Blacks, Japanese and Chinese. Allele alpha LELY occurred in all groups investigated with a fairly uniform frequency: 31%, 21%, 20% and 22%, respectively. Mutations in exon 40 and intron 45 appeared linked to one another without exception. Partial skipping of exon 46 or the low-expression feature, whenever they could be assessed, were invariably observed. Allele alpha LELY appears to be an ancient and stable allele.
α-LELY等位基因是红细胞血影蛋白α链的低表达等位基因。它在第40外显子和第45内含子中均携带突变,并与第46外显子的部分跳跃有关。α-LELY等位基因本身无症状。相反,它会增强反式出现的有害α等位基因的表达水平,因此具有临床重要性。本研究的目的是评估α-LELY等位基因在不同种族群体中的发生率,即白种人、非洲黑人、日本人和中国人。α-LELY等位基因在所有调查的群体中出现的频率相当一致:分别为31%、21%、20%和22%。第40外显子和第45内含子中的突变无一例外似乎相互关联。只要能够评估,第46外显子的部分跳跃或低表达特征总是会被观察到。α-LELY等位基因似乎是一个古老且稳定的等位基因。