Parra Genís, Reymond Alexandre, Dabbouseh Noura, Dermitzakis Emmanouil T, Castelo Robert, Thomson Timothy M, Antonarakis Stylianos E, Guigó Roderic
Grup de Recerca en Informàtica Biomèdica, Institut Municipal d'Investigació Mèdica-Universitat Pompeu Fabra, and Programa de Bioinformàtica i Genòmica, Centre de Regulació Genòmica, E08003 Barcelona, Catalonia, Spain.
Genome Res. 2006 Jan;16(1):37-44. doi: 10.1101/gr.4145906. Epub 2005 Dec 12.
The "one-gene, one-protein" rule, coined by Beadle and Tatum, has been fundamental to molecular biology. The rule implies that the genetic complexity of an organism depends essentially on its gene number. The discovery, however, that alternative gene splicing and transcription are widespread phenomena dramatically altered our understanding of the genetic complexity of higher eukaryotic organisms; in these, a limited number of genes may potentially encode a much larger number of proteins. Here we investigate yet another phenomenon that may contribute to generate additional protein diversity. Indeed, by relying on both computational and experimental analysis, we estimate that at least 4%-5% of the tandem gene pairs in the human genome can be eventually transcribed into a single RNA sequence encoding a putative chimeric protein. While the functional significance of most of these chimeric transcripts remains to be determined, we provide strong evidence that this phenomenon does not correspond to mere technical artifacts and that it is a common mechanism with the potential of generating hundreds of additional proteins in the human genome.
由比德尔和塔特姆提出的“一个基因,一种蛋白质”规则,一直是分子生物学的基础。该规则意味着生物体的遗传复杂性本质上取决于其基因数量。然而,替代基因剪接和转录是普遍现象这一发现,极大地改变了我们对高等真核生物遗传复杂性的理解;在这些生物中,有限数量的基因可能潜在地编码数量多得多的蛋白质。在这里,我们研究了另一种可能有助于产生额外蛋白质多样性的现象。事实上,通过依靠计算和实验分析,我们估计人类基因组中至少4%-5%的串联基因对最终可以转录成一个编码假定嵌合蛋白的RNA序列。虽然这些嵌合转录本中大多数的功能意义仍有待确定,但我们提供了有力证据表明,这一现象并非仅仅是技术假象,而是一种常见机制,有可能在人类基因组中产生数百种额外的蛋白质。