Shneidman P S, Bruce J, Schwartz M L, Schlaepfer W W
Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical School, Philadelphia 19104-6079.
Brain Res Mol Brain Res. 1992 Mar;13(1-2):127-38. doi: 10.1016/0169-328x(92)90052-d.
We have cloned and examined the 5' flanking regions of the heavy (NF-H), light (NF-L) and mid-sized (NF-M) mouse neurofilament (NF) genes in order to begin to characterize the regions of each gene that regulate NF transcription. Chimeric plasmids bearing the CAT reporter gene and deletion mutants of the upstream NF genes were transiently transfected into neuronal (PC12 and Neuro 2A) and non-neuronal (HeLa) cell lines. Constructs bearing upstream regions to -4000 in NF-H, to -5600 in NF-L and to -4500 in NF-M were expressed at low levels in neuronal and in non-neuronal cells. Progressive deletion of 5' flanking sequence to -385 in NF-H, to -325 in NF-L and to -505 in NF-M caused a several-fold increase of transcription from the transfected plasmids. Increases of transcription by deletion mutants followed a similar pattern in neuronal and in non-neuronal cell lines. Negative upstream regions are located between -1314 and -385 in NF-H, between -936 and -325 in NF-L and between -874 and -505 in NF-M. Additional negative regions are present further upstream in NF-L and in NF-H. The negative regions of NF-H and of NF-L suppress transcription when placed in either orientation in front of the SV40 or a heterologous NF promoter. These studies demonstrate that the three mouse NF genes possess similar functional features, namely, that of a relatively strong and promiscuous promoter with negative upstream elements. The role of the negative elements in regulating NF expression remains unclear.
我们克隆并检测了小鼠重链神经丝蛋白(NF-H)、轻链神经丝蛋白(NF-L)和中链神经丝蛋白(NF-M)基因的5'侧翼区,以便开始对调控NF转录的各基因区域进行特征描述。将携带CAT报告基因的嵌合质粒及上游NF基因的缺失突变体瞬时转染至神经元细胞系(PC12和Neuro 2A)和非神经元细胞系(HeLa)。携带NF-H基因上游至-4000区域、NF-L基因上游至-5600区域以及NF-M基因上游至-4500区域的构建体在神经元细胞和非神经元细胞中均低水平表达。将NF-H基因的5'侧翼序列逐步缺失至-385、NF-L基因至-325以及NF-M基因至-505,导致转染质粒的转录增加了数倍。缺失突变体引起的转录增加在神经元细胞系和非神经元细胞系中呈现相似模式。NF-H基因的负上游区域位于-1314至-385之间,NF-L基因位于-936至-325之间,NF-M基因位于-874至-505之间。在NF-L基因和NF-H基因更上游还存在其他负调控区域。当NF-H基因和NF-L基因的负调控区域以任何方向置于SV40或异源NF启动子之前时,均可抑制转录。这些研究表明,三种小鼠NF基因具有相似的功能特征,即具有一个相对较强且具有通用性的启动子以及负上游元件。负调控元件在调节NF表达中的作用仍不清楚。