Button L L, Russell D G, Klein H L, Medina-Acosta E, Karess R E, McMaster W R
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Mol Biochem Parasitol. 1989 Jan 15;32(2-3):271-83. doi: 10.1016/0166-6851(89)90076-5.
The major surface glycoprotein of Leishmania, gp63, is encoded by a small multi-gene family of tandemly linked genes which map to a single chromosome. For Leishmania major, there are five 3.1 kilobasepair (kb) direct repeat units which include a 1.8-kb open reading frame and a 1.3-kb intergenic or spacer region. In addition, there is a single gene copy linked as a direct repeat but separated from the tandem array of gp63 genes by about 8 kb. The restriction enzyme map of the repeat unit is highly conserved among the gene copies. The regions which flank the tandemly repeated genes diverge outside of the 3.1-kb repeat unit. Transcription of the gp63 gene locus is constitutive as the 3-kb transcript was present in promastigotes as well as in amastigotes. A minor 6-kb gp63 gene transcript was also detected in Northern blot analysis which could signify the transcription of the genes as a polycistronic or multigene precursor RNA.
利什曼原虫的主要表面糖蛋白gp63由一个小的多基因家族编码,这些基因串联排列在一条染色体上。对于硕大利什曼原虫,有五个3.1千碱基对(kb)的直接重复单元,包括一个1.8 kb的开放阅读框和一个1.3 kb的基因间或间隔区。此外,还有一个单一的基因拷贝以直接重复的形式连接,但与gp63基因的串联阵列相隔约8 kb。重复单元的限制性内切酶图谱在基因拷贝中高度保守。串联重复基因两侧的区域在3.1 kb重复单元之外存在差异。gp63基因座的转录是组成型的,因为在前鞭毛体和无鞭毛体中都存在3 kb的转录本。在Northern印迹分析中还检测到一个较小的6 kb gp63基因转录本,这可能意味着这些基因作为多顺反子或多基因前体RNA进行转录。