Li W, Mathews C, Gao C, DenBesten P K
Department of Growth and Development, University of California at San Francisco 94143-0640, USA.
Arch Oral Biol. 1998 Jun;43(6):497-504. doi: 10.1016/s0003-9969(98)00013-2.
Alternative splicing of the amelogenin gene generates a family of proteins secreted by ameloblasts that are primarily responsible for tooth enamel formation. Here the presence of two additional exons, downstream of exon 7, which are followed by an alternate polyadenylation site, is reported. Long polymerase chain reaction was used with a rat genomic amelogenin template to amplify sequences downstream from the primary polyadenylation site. Within the amplified sequences, two exons of 45 bp (exon 8) and 110 bp (exon 9) were identified. The presence of these additional exons in the human and mouse genome was indicated by Southern blot analysis. Antibodies raised against a synthetic peptide corresponding to a sequence encoded by exon 9 positively stained ameloblasts in sections of developing murine and porcine unerupted teeth. These results suggest that an amelogenin protein(s) that includes sequences derived from exons 8 and 9 is synthesized by the ameloblasts.
釉原蛋白基因的可变剪接产生了一个由成釉细胞分泌的蛋白质家族,这些蛋白质主要负责牙釉质的形成。本文报道了在第7外显子下游存在另外两个外显子,其后面跟着一个可变聚腺苷酸化位点。使用大鼠基因组釉原蛋白模板进行长链聚合酶链反应,以扩增初级聚腺苷酸化位点下游的序列。在扩增序列中,鉴定出两个分别为45 bp(第8外显子)和110 bp(第9外显子)的外显子。Southern印迹分析表明人类和小鼠基因组中存在这些额外的外显子。针对与第9外显子编码序列对应的合成肽产生的抗体,在发育中的小鼠和猪未萌出牙的切片中对成釉细胞进行了阳性染色。这些结果表明,成釉细胞合成了一种包含来自第8和第9外显子序列的釉原蛋白。