Virbasius J V, Scarpulla R C
Department of Cell, Molecular and Structural Biology, Northwestern University Medical School, Chicago, IL 60611.
Nucleic Acids Res. 1990 Nov 25;18(22):6581-6. doi: 10.1093/nar/18.22.6581.
We have isolated three members of the rat cytochrome c oxidase subunit IV gene family: one functional gene and two processed pseudogenes. The pseudogenes appear to represent the only other closely related sequences in this family. The functional gene encodes an isoform which is expressed in all tissues examined and has features characteristic of 'housekeeping' genes. These include multiple transcription start sites mapped to within an approximately 50 bp region and a GC-rich promoter lacking typical CCAAT or TATAA sequences. Although the subunit IV gene is expressed at its highest levels in cardiac and skeletal muscle, consistent with the high energy demand in those tissues, its expression differs from that of cytochrome c in several respects. 1) Subunit IV mRNA abundance in various tissues is relatively uniform when compared to the highly variable levels of cytochrome c mRNAs. 2) Unlike cytochrome c, subunit IV mRNA is expressed at a surprisingly high level in testis. 3) While cytochrome c mRNA levels in liver are increased markedly in response to thyroid hormone treatment, subunit IV mRNA is not significantly affected. Differences in the expression of these two nuclear-encoded respiratory genes are consistent with differences in regulatory elements within their promoters. Therefore, the regulation of nuclear-encoded respiratory genes in response to tissue demands for cellular energy may not be satisfactorily explained by a set of universal regulators common to all such genes.
我们已经分离出大鼠细胞色素c氧化酶亚基IV基因家族的三个成员:一个功能基因和两个加工假基因。这些假基因似乎代表了该家族中仅有的其他密切相关序列。该功能基因编码一种在所有检测组织中均有表达的同工型,具有“管家”基因的特征。这些特征包括多个转录起始位点定位在大约50bp的区域内,以及一个富含GC的启动子,缺乏典型的CCAAT或TATAA序列。尽管亚基IV基因在心脏和骨骼肌中表达水平最高,这与这些组织中的高能量需求一致,但其表达在几个方面与细胞色素c不同。1)与细胞色素c mRNA高度可变的水平相比,亚基IV mRNA在各种组织中的丰度相对均匀。2)与细胞色素c不同,亚基IV mRNA在睾丸中以惊人的高水平表达。3)虽然甲状腺激素处理后肝脏中的细胞色素c mRNA水平显著增加,但亚基IV mRNA不受明显影响。这两个核编码呼吸基因表达的差异与它们启动子内调控元件的差异一致。因此,对于核编码呼吸基因响应组织对细胞能量需求的调控,可能无法用所有此类基因共有的一组通用调节因子来令人满意地解释。