Meakin S O, Du R P, Tsui L C, Breitman M L
Department of Medical Genetics and Medical Biophysics, University of Toronto, Ontario, Canada.
Mol Cell Biol. 1987 Aug;7(8):2671-9. doi: 10.1128/mcb.7.8.2671-2679.1987.
While only two gamma-crystallins have been identified in the human eye lens, molecular studies indicate that the human gamma-crystallins are encoded in a multigene family comprising at least seven closely related members. Sequence analysis of five of these genes has suggested that three (gamma 1-2, G3, and G4) are potentially active, while two (G1 psi and G2 psi) correspond to closely related pseudogenes. Here we report on the detailed structure of a sixth gamma-crystallin gene, G5, and our results obtained with transient expression assays to characterize both the promoter activity and translation products of five members of the gene family. We show that 5'-flanking sequences of G1 psi and G2 psi lacked detectable promoter activity, while the corresponding sequences of G3, G4, and G5 were able to direct high levels of expression of the bacterial chloramphenicol acetyltransferase gene in primary lens epithelia, but not in cultures of nonlens origin. Detailed sequence comparisons indicated that active genes contained several conserved sequence tracts 5' of the TATA box which may constitute functional elements of a lens-specific gamma-crystallin promoter. Expression of the gamma-crystallin coding sequences from the human metallothionein IIA promoter in nonlens cells facilitated characterization of the polypeptides encoded by individual gamma-genes and, in future studies, should permit comparison of these proteins with distinct gamma-crystallins in the human lens.
虽然在人眼晶状体中仅鉴定出两种γ-晶状体蛋白,但分子研究表明,人γ-晶状体蛋白由一个多基因家族编码,该家族至少包含七个密切相关的成员。对其中五个基因的序列分析表明,三个基因(γ1-2、G3和G4)可能具有活性,而另外两个基因(G1 psi和G2 psi)对应于密切相关的假基因。在此,我们报告第六个γ-晶状体蛋白基因G5的详细结构,以及我们通过瞬时表达分析获得的结果,以表征该基因家族五个成员的启动子活性和翻译产物。我们发现,G1 psi和G2 psi的5'侧翼序列缺乏可检测到的启动子活性,而G3、G4和G5的相应序列能够在原代晶状体上皮细胞中指导细菌氯霉素乙酰转移酶基因的高水平表达,但在非晶状体来源的培养物中则不能。详细的序列比较表明,活性基因在TATA框的5'端含有几个保守的序列片段,这些片段可能构成晶状体特异性γ-晶状体蛋白启动子的功能元件。在非晶状体细胞中,从人金属硫蛋白IIA启动子表达γ-晶状体蛋白编码序列有助于表征各个γ-基因编码的多肽,并且在未来的研究中,应该能够将这些蛋白质与人晶状体中不同的γ-晶状体蛋白进行比较。