Avraham S, Stevens R L, Gartner M C, Austen K F, Lalley P A, Weis J H
Department of Medicine, Harvard Medical School, Boston, Massachusetts.
J Biol Chem. 1988 May 25;263(15):7292-6.
It has been previously shown that a single gene is used to encode the peptide core of the extracellular proteoglycan of rat L2 yolk sac tumor cells and the intracellular proteoglycan of rat basophilic leukemia (RBL)-1 cells. In order to determine if the predicted amino acid sequences of these proteoglycans are identical as well as to isolate a full length cDNA encoding a rat secretory granule proteoglycan, a cDNA library was prepared from RBL-1 cells and screened with the 165-base pair 5'----XmnI fragment of pPG-1, a partial cDNA which encodes the rat L2 cell proteoglycan peptide core. Based on the consensus nucleotide sequence of two full length RBL-1 cell-derived cDNAs, the 5' untranslated region of the mRNA that is expressed in RBL-1 cells is shorter than that expressed in the rat L2 cells although the coding regions of the mRNAs from the two cell types are identical. These findings indicate that the targeting of proteoglycans to an intracellular or extracellular compartment is a cell-specific event which is independent of the translated peptide core. Since the RBL-1 cell and the rat L2 cell proteoglycans have different types of glycosaminoglycans bound to them, it can also be concluded that the selection of the type of glycosaminoglycan that will be synthesized onto a peptide core is a cell-specific event which is not exclusively dependent on the translated peptide core. When the predicted amino acid sequence of the RBL-1 cell proteoglycan peptide core was compared to the predicted sequence of the homologous human molecule from HL-60 cells, 48% of the amino acids were identical. The N terminus was the most highly conserved area of the molecule. This region of the peptide core, which precedes the serine-glycine repeat region, is likely to be of critical importance for the biosynthesis and/or function of these proteoglycans. Analysis of 10 different mouse/hamster somatic cell hybrid lines with a SspI----3' fragment of the rat L2 cell cDNA revealed that, as in the human, the gene that encodes the mouse analogue of this peptide core resides on chromosome 10.
先前已经表明,单个基因用于编码大鼠L2卵黄囊肿瘤细胞的细胞外蛋白聚糖和大鼠嗜碱性白血病(RBL)-1细胞的细胞内蛋白聚糖的肽核心。为了确定这些蛋白聚糖的预测氨基酸序列是否相同,并分离编码大鼠分泌颗粒蛋白聚糖的全长cDNA,从RBL-1细胞制备了cDNA文库,并用pPG-1的165个碱基对的5'----XmnI片段进行筛选,pPG-1是一个部分cDNA,编码大鼠L2细胞蛋白聚糖肽核心。基于两个全长RBL-1细胞来源的cDNA的共有核苷酸序列,RBL-1细胞中表达的mRNA的5'非翻译区比大鼠L2细胞中表达的短,尽管两种细胞类型的mRNA的编码区是相同的。这些发现表明,蛋白聚糖靶向细胞内或细胞外区室是一个细胞特异性事件,与翻译后的肽核心无关。由于RBL-1细胞和大鼠L2细胞的蛋白聚糖结合有不同类型的糖胺聚糖,还可以得出结论,选择将在肽核心上合成的糖胺聚糖类型是一个细胞特异性事件,并不完全依赖于翻译后的肽核心。当将RBL-1细胞蛋白聚糖肽核心的预测氨基酸序列与来自HL-60细胞的同源人类分子的预测序列进行比较时,48%的氨基酸是相同的。N末端是分子中保守性最高的区域。肽核心的这个区域在丝氨酸-甘氨酸重复区域之前,可能对这些蛋白聚糖的生物合成和/或功能至关重要。用大鼠L2细胞cDNA的SspI----3'片段分析10种不同的小鼠/仓鼠体细胞杂交系表明,与人类一样,编码该肽核心小鼠类似物的基因位于10号染色体上。