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Letter
Nature Genetics  31, 415 - 418 (2002)
Published online: 22 July 2002; | doi:10.1038/ng940

Selection for short introns in highly expressed genes

Cristian I. Castillo-Davis1, Sergei L. Mekhedov2, Daniel L. Hartl1, Eugene V. Koonin2 & Fyodor A. Kondrashov2

1  Department of Organismic and Evolutionary Biology, Harvard University, 16 Divinity Avenue, Cambridge, Massachusetts 02138, USA.

2  National Center for Biotechnology Information, National Institutes of Health, 8600 Rockville Pike, Bethesda, Maryland 20894, USA.

Correspondence should be addressed to Fyodor A. Kondrashov fkondras@ncbi.nlm.nih.gov
Transcription is a slow and expensive process: in eukaryotes, approximately 20 nucleotides can be transcribed per second1, 2 at the expense of at least two ATP molecules per nucleotide3. Thus, at least for highly expressed genes, transcription of long introns, which are particularly common in mammals, is costly. Using data on the expression of genes that encode proteins in Caenorhabditis elegans and Homo sapiens, we show that introns in highly expressed genes are substantially shorter than those in genes that are expressed at low levels. This difference is greater in humans, such that introns are, on average, 14 times shorter in highly expressed genes than in genes with low expression, whereas in C. elegans the difference in intron length is only twofold. In contrast, the density of introns in a gene does not strongly depend on the level of gene expression. Thus, natural selection appears to favor short introns in highly expressed genes to minimize the cost of transcription and other molecular processes, such as splicing.


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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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