Tang T K, Leto T L, Correas I, Alonso M A, Marchesi V T, Benz E J
Department of Human Genetics, School of Medicine, Yale University, New Haven, CT 06510.
Proc Natl Acad Sci U S A. 1988 Jun;85(11):3713-7. doi: 10.1073/pnas.85.11.3713.
We have conducted comparative analysis of nucleotide sequences encoding erythroid and lymphoid protein 4.1 isoforms. The lymphoid protein 4.1 isoforms exhibit several nucleotide sequence motifs that appear to be either inserted into or deleted from the mRNA sequence by alternative splicing of a common mRNA precursor. One of these motifs, located within the spectrin-actin binding domain, is found only in erythroid cells and is specifically produced during erythroid cell maturation. The selective expression of the alternatively spliced mRNA during erythroid maturation implies the existence of a lineage-specific splicing mechanism whose activity is triggered by terminal maturation.
我们对编码红细胞和淋巴细胞蛋白4.1亚型的核苷酸序列进行了比较分析。淋巴细胞蛋白4.1亚型表现出几个核苷酸序列基序,这些基序似乎是通过共同mRNA前体的可变剪接插入或从mRNA序列中删除的。其中一个基序位于血影蛋白-肌动蛋白结合域内,仅在红细胞中发现,并在红细胞成熟过程中特异性产生。可变剪接mRNA在红细胞成熟过程中的选择性表达意味着存在一种谱系特异性剪接机制,其活性由终末成熟触发。