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转录因子数量的编码限制。

Coding limits on the number of transcription factors.

作者信息

Itzkovitz Shalev, Tlusty Tsvi, Alon Uri

机构信息

Dept Molecular Cell Biology, Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

BMC Genomics. 2006 Sep 19;7:239. doi: 10.1186/1471-2164-7-239.

Abstract

BACKGROUND

Transcription factor proteins bind specific DNA sequences to control the expression of genes. They contain DNA binding domains which belong to several super-families, each with a specific mechanism of DNA binding. The total number of transcription factors encoded in a genome increases with the number of genes in the genome. Here, we examined the number of transcription factors from each super-family in diverse organisms.

RESULTS

We find that the number of transcription factors from most super-families appears to be bounded. For example, the number of winged helix factors does not generally exceed 300, even in very large genomes. The magnitude of the maximal number of transcription factors from each super-family seems to correlate with the number of DNA bases effectively recognized by the binding mechanism of that super-family. Coding theory predicts that such upper bounds on the number of transcription factors should exist, in order to minimize cross-binding errors between transcription factors. This theory further predicts that factors with similar binding sequences should tend to have similar biological effect, so that errors based on mis-recognition are minimal. We present evidence that transcription factors with similar binding sequences tend to regulate genes with similar biological functions, supporting this prediction.

CONCLUSION

The present study suggests limits on the transcription factor repertoire of cells, and suggests coding constraints that might apply more generally to the mapping between binding sites and biological function.

摘要

背景

转录因子蛋白通过结合特定的DNA序列来控制基因的表达。它们包含属于几个超家族的DNA结合结构域,每个超家族都有特定的DNA结合机制。基因组中编码的转录因子总数随着基因组中基因数量的增加而增加。在此,我们研究了不同生物体中每个超家族的转录因子数量。

结果

我们发现,大多数超家族的转录因子数量似乎是有限的。例如,即使在非常大的基因组中,有翼螺旋因子的数量通常也不会超过300个。每个超家族转录因子的最大数量似乎与该超家族结合机制有效识别的DNA碱基数量相关。编码理论预测,转录因子数量的这种上限应该存在,以便将转录因子之间的交叉结合错误降至最低。该理论进一步预测,具有相似结合序列的因子应该倾向于具有相似的生物学效应,从而使基于错误识别的错误最小化。我们提供的证据表明,具有相似结合序列的转录因子倾向于调控具有相似生物学功能的基因,支持了这一预测。

结论

本研究表明了细胞转录因子库的限制,并提出了可能更广泛适用于结合位点与生物学功能之间映射的编码限制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fd1/1590034/f1aac1710019/1471-2164-7-239-1.jpg

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