Ishii Kyota, Washio Takanori, Uechi Tamayo, Yoshihama Maki, Kenmochi Naoya, Tomita Masaru
Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata 997-0035, Japan.
BMC Genomics. 2006 Feb 28;7:37. doi: 10.1186/1471-2164-7-37.
The ribosome is a central player in the translation system, which in mammals consists of four RNA species and 79 ribosomal proteins (RPs). The control mechanisms of gene expression and the functions of RPs are believed to be identical. Most RP genes have common promoters and were therefore assumed to have a unified gene expression control mechanism.
We systematically analyzed the homogeneity and heterogeneity of RP genes on the basis of their expression profiles, promoter structures, encoded amino acid compositions, and codon compositions. The results revealed that (1) most RP genes are coordinately expressed at the mRNA level, with higher signals in the spleen, lymph node dissection (LND), and fetal brain. However, 17 genes, including the P protein genes (RPLP0, RPLP1, RPLP2), are expressed in a tissue-specific manner. (2) Most promoters have GC boxes and possible binding sites for nuclear respiratory factor 2, Yin and Yang 1, and/or activator protein 1. However, they do not have canonical TATA boxes. (3) Analysis of the amino acid composition of the encoded proteins indicated a high lysine and arginine content. (4) The major RP genes exhibit a characteristic synonymous codon composition with high rates of G or C in the third-codon position and a high content of AAG, CAG, ATC, GAG, CAC, and CTG.
Eleven of the RP genes are still identified as being unique and did not exhibit at least some of the above characteristics, indicating that they may have unknown functions not present in other RP genes. Furthermore, we found sequences conserved between human and mouse genes around the transcription start sites and in the intronic regions. This study suggests certain overall trends and characteristic features of human RP genes.
核糖体是翻译系统的核心组成部分,在哺乳动物中,它由四种RNA和79种核糖体蛋白(RP)组成。人们认为基因表达的调控机制和核糖体蛋白的功能是相同的。大多数核糖体蛋白基因具有共同的启动子,因此假定它们具有统一的基因表达调控机制。
我们基于核糖体蛋白基因的表达谱、启动子结构、编码氨基酸组成和密码子组成,系统地分析了它们的同质性和异质性。结果显示:(1)大多数核糖体蛋白基因在mRNA水平上协同表达,在脾脏、淋巴结清扫组织(LND)和胎儿脑中信号较高。然而,包括P蛋白基因(RPLP0、RPLP1、RPLP2)在内的17个基因以组织特异性方式表达。(2)大多数启动子具有GC盒以及核呼吸因子2、阴阳1和/或激活蛋白1的可能结合位点。然而,它们没有典型的TATA盒。(3)对编码蛋白的氨基酸组成分析表明赖氨酸和精氨酸含量较高。(4)主要的核糖体蛋白基因表现出特征性的同义密码子组成,在密码子第三位G或C的使用率较高,并且AAG、CAG、ATC、GAG、CAC和CTG的含量较高。
仍有11个核糖体蛋白基因被鉴定为独特的,并且至少没有表现出上述某些特征,这表明它们可能具有其他核糖体蛋白基因所没有的未知功能。此外,我们发现在转录起始位点周围和内含子区域,人类和小鼠基因之间存在保守序列。这项研究揭示了人类核糖体蛋白基因的某些总体趋势和特征。