Relationship between the total size of exons and introns in protein-coding genes of higher eukaryotes
- PMID: 6959108
- PMCID: PMC347086
- DOI: 10.1073/pnas.79.20.6196
Relationship between the total size of exons and introns in protein-coding genes of higher eukaryotes
Abstract
We have attempted to ascertain the correlation between the genetic information content in the exons and the surrounding intron sequences with regard to their spatial arrangement within a gene. A comparison is made of the sizes, taken from recent publications, of exons and introns of approximately equal to 80 different protein-coding chromosomal genes, mostly from higher eukaryotes. The exons of these genes do not show very marked variation in size and can be classified into three major discrete and two minor additional size groups, whereas individual introns vary considerably in size within and between genes. Notwithstanding, the overall length of all introns present within a given gene is a function of the total size, mostly corresponding to the total genetic information content, of the exons. Three cases that violate this exon-size dependency of introns are genes coding for (i) histone H1, feather keratin, and interferons, (ii) tubulin and actin, and (iii) silk fibroin. The exons of these genes are larger than 0.7 kilobase pair in total size and the genes show a strong sequence homogeneity among the repetitious family members or internal repeats of coding sequences within the gene. We propose that conservation of sequences, which is required by the family members, internal repeats, or the entire gene, would actually motivate the removal of introns.
Similar articles
-
The 5' leader of plant PgiC has an intron: the leader shows both the loss and maintenance of constraints compared with introns and exons in the coding region.Mol Biol Evol. 2002 Sep;19(9):1613-23. doi: 10.1093/oxfordjournals.molbev.a004223. Mol Biol Evol. 2002. PMID: 12200488
-
Exon/intron organization of the chicken type II procollagen gene: intron size distribution suggests a minimal intron size.Proc Natl Acad Sci U S A. 1986 Apr;83(8):2325-9. doi: 10.1073/pnas.83.8.2325. Proc Natl Acad Sci U S A. 1986. PMID: 3010306 Free PMC article.
-
Characterization of bovine keratin genes: similarities of exon patterns in genes coding for different keratins.EMBO J. 1984 Dec 20;3(13):3279-87. doi: 10.1002/j.1460-2075.1984.tb02290.x. EMBO J. 1984. PMID: 6084595 Free PMC article.
-
Whence genes in pieces: reconstruction of the exon-intron gene structures of the last eukaryotic common ancestor and other ancestral eukaryotes.Wiley Interdiscip Rev RNA. 2013 Jan-Feb;4(1):93-105. doi: 10.1002/wrna.1143. Epub 2012 Nov 8. Wiley Interdiscip Rev RNA. 2013. PMID: 23139082 Review.
-
Evolutionarily mobile modules in proteins.Sci Am. 1993 Oct;269(4):50-6. doi: 10.1038/scientificamerican1093-50. Sci Am. 1993. PMID: 8235550 Review. No abstract available.
Cited by
-
On the nature of the Duchenne muscular dystrophy locus: a portion of a complex of related gene clusters of recent pseudoautosomal origin?Mol Cell Biochem. 1988 Jun;81(2):103-19. doi: 10.1007/BF00219313. Mol Cell Biochem. 1988. PMID: 3050449 Review.
-
Complete sequence of a bovine type I cytokeratin gene: conserved and variable intron positions in genes of polypeptides of the same cytokeratin subfamily.EMBO J. 1985 Sep;4(9):2261-7. doi: 10.1002/j.1460-2075.1985.tb03924.x. EMBO J. 1985. PMID: 2416562 Free PMC article.
-
Comparative genome analysis of cortactin and HS1: the significance of the F-actin binding repeat domain.BMC Genomics. 2005 Feb 14;6:15. doi: 10.1186/1471-2164-6-15. BMC Genomics. 2005. PMID: 15710041 Free PMC article.
-
Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndrome.Mamm Genome. 1996 Dec;7(12):911-4. doi: 10.1007/s003359900268. Mamm Genome. 1996. PMID: 8995764 No abstract available.
-
Evolution of chick type I procollagen genes.J Mol Evol. 1985;22(3):209-19. doi: 10.1007/BF02099750. J Mol Evol. 1985. PMID: 3935803
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical