Stamm S, Casper D, Dinsmore J, Kaufmann C A, Brosius J, Helfman D M
Fishberg Research Center in Neurobiology, Mount Sinai School of Medicine, New York, NY 10029.
Nucleic Acids Res. 1992 Oct 11;20(19):5097-103. doi: 10.1093/nar/20.19.5097.
The clathrin light chains are components of clathrin coated vesicles, structural constituents involved in endocytosis and membrane recycling. The clathrin light chain B (LCB) gene encodes two isoforms, termed LCB2 and LCB3, via an alternative RNA splicing mechanism. We have determined the structure of the rat clathrin light chain B gene. The gene consists of six exons that extend over 11.9 kb. The first four exons and the last exon are common to the LCB2 and LCB3 isoforms. The fifth exon, termed EN, is included in the mRNA in brain, giving rise to the brain specific form LCB2 but is excluded in other tissues, generating the LCB3 isoform. Primary rat neuronal cell cultures express predominantly the brain specific LCB2 isoform, whereas primary rat cultures of glia express only the LCB3 isoform, suggesting that expression of the brain-specific LCB2 form is limited to neurons. Further evidence for neuronal localization of the LCB2 form is provided using a teratocarcinoma cell line, P19, which can be induced by retinoic acid to express a neuronal phenotype, concomitant with the induction of the LCB2 form. In order to determine the sequences involved in alternative splice site selection, we constructed a minigene containing the alternative spliced exon EN and its flanking intron and exon sequences. This minigene reflects the splicing pattern of the endogenous gene upon transfection in HeLa cell and primary neuronal cell cultures, indicating that this region of the LCB gene contains all the necessary information for neuron-specific splicing.
网格蛋白轻链是网格蛋白包被小泡的组成成分,是参与内吞作用和膜循环的结构成分。网格蛋白轻链B(LCB)基因通过可变RNA剪接机制编码两种异构体,称为LCB2和LCB3。我们已经确定了大鼠网格蛋白轻链B基因的结构。该基因由六个外显子组成,跨越11.9 kb。前四个外显子和最后一个外显子是LCB2和LCB3异构体共有的。第五个外显子,称为EN,包含在大脑中的mRNA中,产生大脑特异性形式LCB2,但在其他组织中被排除,产生LCB3异构体。原代大鼠神经元细胞培养物主要表达大脑特异性LCB2异构体,而原代大鼠神经胶质细胞培养物仅表达LCB3异构体,这表明大脑特异性LCB2形式的表达仅限于神经元。使用畸胎瘤细胞系P19提供了LCB2形式神经元定位的进一步证据,该细胞系可被视黄酸诱导表达神经元表型,并伴随LCB2形式的诱导。为了确定参与可变剪接位点选择的序列,我们构建了一个小基因,该小基因包含可变剪接的外显子EN及其侧翼内含子和外显子序列。该小基因反映了内源性基因在转染到HeLa细胞和原代神经元细胞培养物中的剪接模式,表明LCB基因的该区域包含神经元特异性剪接所需的所有信息。