Maillet P, Dalla Venezia N, Bozon M, Vallier A, Delaunay J, Baklouti F
Génétique Moléculaire Humaine, CNRS URA 1171, Institut Pasteur de Lyon, France.
Hum Mutat. 1998;11(4):342-3.
Protein 4.1 is a major component of the junctional complex at the red cell skeleton. Genomic studies have recently evidenced that the encoding gene (EL1 locus) is present in a single copy per haploid genome. Several RFLPs have already been characterized within intron sequences. Here, we describe the first RFLP found within the coding sequence. This polymorphism (C or T at position 2723, in exon 21) does not affect the amino acid sequence (Thr-->Thr). It can be detected by either Dde I restriction digestion of an appropriate PCR product, or simply by SSCP These findings should facilitate analysis of families with 4.1 deficiencies causing hereditary elliptocytosis.
蛋白质4.1是红细胞骨架连接复合体的主要成分。基因组研究最近证明,编码基因(EL1位点)在每个单倍体基因组中以单拷贝形式存在。几个限制性片段长度多态性(RFLP)已在基因内序列中得到鉴定。在此,我们描述了在编码序列中发现的首个RFLP。这种多态性(第21外显子第2723位为C或T)不影响氨基酸序列(苏氨酸→苏氨酸)。它可以通过对合适的聚合酶链反应(PCR)产物进行Dde I限制性酶切检测,或者简单地通过单链构象多态性(SSCP)检测。这些发现应有助于对因4.1缺乏导致遗传性椭圆形红细胞增多症的家系进行分析。