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Isolation of cellular genes differentially expressed in mouse NIH 3T3 cells and a simian virus 40-transformed derivative: growth-specific expression of VL30 genes.

机译:小鼠NIH 3T3细胞和猿猴病毒40转化衍生物中差异表达的细胞基因的分离:VL30基因的生长特异性表达。

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摘要

We constructed and screened a cDNA library made from simian virus 40 (SV40)-transformed NIH 3T3 cells, and we isolated cDNAs representing genes that are differentially expressed between the parental cell and its SV40-transformed derivative. We found only a small number of cDNAs representing such genes. Two isolated cDNA clones represented RNAs expressed at elevated levels in the transformed cell line in a manner relatively independent of growth conditions. The expression of two other cDNAs was growth specific because transformed cells and nonconfluent parental cells contained higher levels of the homologous RNAs than did confluent, contact-inhibited parental cells. Another cDNA was well expressed in confluent parental and confluent transformed cells, but not in nonconfluent cells. The expression of some of these cDNAs varied strikingly in different mouse cell lines. Thus the genotype or histories of different cell lines can also affect the expression of certain genes. Interestingly, the only cDNA isolated that was expressed exclusively in the transformed cell was from an SV40 message. We focused on a growth-specific cDNA which we show is derived from a mouse endogenous retrovirus-like family called VL30. We sequenced the 3' long terminal repeat (LTR) of this transcriptionally active VL30 gene. This LTR has good homology with other VL30 LTR sequences, but differences occur, particularly upstream of the VL30 promoter. We found that VL30 gene expression varied in different mouse cell lines such that C3H cell lines had very low levels of VL30 transcripts relative to NIH 3T3 cell lines. However, Southern analysis showed that both cell lines had about the same number of VL30 genes homologous to our probe and that the position of the majority of these genes was conserved. We discuss possible explanations for this difference in VL30 expression.
机译:我们构建并筛选了由猿猴病毒40(SV40)转化的NIH 3T3细胞制成的cDNA文库,并分离了代表在亲代细胞及其SV40转化的衍生物之间差异表达的基因的cDNA。我们只发现了代表这些基因的少数cDNA。两个分离的cDNA克隆代表以相对独立于生长条件的方式在转化的细胞系中以高水平表达的RNA。另外两个cDNA的表达具有生长特异性,因为转化的细胞和非融合的亲代细胞比接触抑制的融合亲代细胞含有更高水平的同源RNA。另一个cDNA在融合的亲本和融合转化细胞中表达良好,但在非融合细胞中却没有表达。其中一些cDNA的表达在不同的小鼠细胞系中显着变化。因此,不同细胞系的基因型或历史也可以影响某些基因的表达。有趣的是,唯一在转化细胞中唯一表达的cDNA是来自SV40信息。我们专注于生长特异性的cDNA,我们显示它来自称为VL30的小鼠内源性逆转录病毒样家族。我们对该转录活性VL30基因的3'长末端重复序列(LTR)进行了测序。该LTR与其他VL30 LTR序列具有良好的同源性,但是发生差异,特别是在VL30启动子的上游。我们发现VL30基因表达在不同的小鼠细胞系中有所不同,因此相对于NIH 3T3细胞系,C3H细胞系的VL30转录物水平非常低。但是,Southern分析显示,两种细胞系都具有与我们的探针同源的大约相同数量的VL30基因,并且大多数这些基因的位置均是保守的。我们讨论了VL30表达差异的可能解释。

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