Lum L S, Dovc P, Medrano J F
Department of Animal Science, University of California, Davis 95616-8521, USA.
J Dairy Sci. 1997 Jul;80(7):1389-97. doi: 10.3168/jds.S0022-0302(97)76068-5.
Differential production of the two most common allelic variants of beta-lactoglobulin (LG), beta-LG A and beta-LG B, has been observed using PAGE. This study evaluated 733 bp of the beta-LG promoter region and 92 bp of the first exon for possible polymorphisms using denaturing gradient gel electrophoresis and nucleotide sequence analysis. Within this region, 13 single nucleotide substitution polymorphisms were detected. Twelve polymorphisms were allele specific, and one appeared to be polymorphic only for the B allele. Several potential binding sites for transcription factors were found within the promoter sequence. This study investigated the role of the G to C transversion within a consensus binding site for activator protein-2 at position-430 bp upstream from the transcription initiation site. Using the DNase-I footprint assay, we confirmed the functional importance of this point mutation and showed different binding affinities of activator protein-2 for both alleles. We discuss the possible regulatory role of activator protein-2 in the transcriptional regulation of the beta-LG gene and propose the activator protein-2 transcription factor as a modulator of gene expression of beta-LG.
利用聚丙烯酰胺凝胶电泳(PAGE)已观察到β-乳球蛋白(LG)两种最常见等位基因变体β-LG A和β-LG B的差异表达。本研究使用变性梯度凝胶电泳和核苷酸序列分析,评估了β-LG启动子区域的733 bp和第一个外显子的92 bp是否存在多态性。在该区域内,检测到13个单核苷酸替代多态性。其中12个多态性是等位基因特异性的,有一个似乎仅对B等位基因呈多态性。在启动子序列中发现了几个潜在的转录因子结合位点。本研究调查了转录起始位点上游430 bp处激活蛋白-2共有结合位点内G到C的颠换作用。使用DNA酶I足迹试验,我们证实了该点突变的功能重要性,并显示激活蛋白-2对两个等位基因具有不同的结合亲和力。我们讨论了激活蛋白-2在β-LG基因转录调控中可能的调节作用,并提出激活蛋白-2转录因子作为β-LG基因表达的调节剂。