ArticleNucleic acids research2001
Digging for dead genes: an analysis of the characteristics of the pseudogene population in the Caenorhabditis elegans genome.
Article in Nucleic acids research, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.
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Who cites it
41 citing papers in PubMed, 124 citations in OpenAlex.
- A large-scale phylogeny-guided analysis of pseudogenes inMicrobiology spectrum · 2023Article
- The pseudogene problem and RT-qPCR data normalization; SYMPK: a suitable reference gene for papillary thyroid carcinoma.Scientific reports · 2020Article
- dreamBase: DNA modification, RNA regulation and protein binding of expressed pseudogenes in human health and disease.Nucleic acids research · 2018Article
- Pseudogenes and Their Genome-Wide Prediction in Plants.International journal of molecular sciences · 2016Review
- Nucleosome Organization around Pseudogenes in the Human Genome.BioMed research international · 2015Article
- Gene-pseudogene evolution: a probabilistic approach.BMC genomics · 2015Article
- Comparative analysis of pseudogenes across three phyla.Proceedings of the National Academy of Sciences of the United States of America · 2014Article
- Trichinella pseudospiralis vs. T. spiralis thymidylate synthase gene structure and T. pseudospiralis thymidylate synthase retrogene sequence.Parasites & vectors · 2014Article
- Human Transcriptome and Chromatin Modifications: An ENCODE Perspective.Genomics & informatics · 2013Article
- The GENCODE pseudogene resource.Genome biology · 2012Article
- Pseudogenes: pseudo-functional or key regulators in health and disease?RNA (New York, N.Y.) · 2011Review
- Two complementary recessive genes in duplicated segments control etiolation in rice.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2011Article
- The ABC transporter gene family of Daphnia pulex.BMC genomics · 2009Article
- Comparative genomics and molecular dynamics of DNA repeats in eukaryotes.Microbiology and molecular biology reviews : MMBR · 2008Review
- Retrosequence formation restructures the yeast genome.Genes & development · 2007Article
- FGF: a web tool for Fishing Gene Family in a whole genome database.Nucleic acids research · 2007Article
- Gene decay in archaea.Archaea (Vancouver, B.C.) · 2007Article
- Origins and impact of constraints in evolution of gene families.Genome research · 2006Article
- Processed pseudogenes, processed genes, and spontaneous mutations in the Arabidopsis genome.Journal of molecular evolution · 2006Article
- Positive and negative selection in the beta-esterase gene cluster of the Drosophila melanogaster subgroup.Journal of molecular evolution · 2006Article
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3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pseudogenes are non-functioning copies of genes in genomic DNA, which may either result from reverse transcription from an mRNA transcript (processed pseudogenes) or from gene duplication and subsequent disablement (non-processed pseudogenes). As pseudogenes are apparently 'dead', they usually have a variety of obvious disablements (e.g., insertions, deletions, frameshifts and truncations) relative to their functioning homologs. We have derived an initial estimate of the size, distribution and characteristics of the pseudogene population in the Caenorhabditis elegans genome, performing a survey in 'molecular archaeology'. Corresponding to the 18 576 annotated proteins in the worm (i.e., in Wormpep18), we have found an estimated total of 2168 pseudogenes, about one for every eight genes. Few of these appear to be processed. Details of our pseudogene assignments are available from http://bioinfo.mbb.yale.edu/genome/worm/pseudogene. The population of pseudogenes differs significantly from that of genes in a number of respects: (i) pseudogenes are distributed unevenly across the genome relative to genes, with a disproportionate number on chromosome IV; (ii) the density of pseudogenes is higher on the arms of the chromosomes; (iii) the amino acid composition of pseudogenes is midway between that of genes and (translations of) random intergenic DNA, with enrichment of Phe, Ile, Leu and Lys, and depletion of Asp, Ala, Glu and Gly relative to the worm proteome; and (iv) the most common protein folds and families differ somewhat between genes and pseudogenes-whereas the most common fold found in the worm proteome is the immunoglobulin fold and the most common 'pseudofold' is the C-type lectin. In addition, the size of a gene family bears little overall relationship to the size of its corresponding pseudogene complement, indicating a highly dynamic genome. There are in fact a number of families associated with large populations of pseudogenes. For example, one family of seven-transmembrane receptors (represented by gene B0334.7) has one pseudogene for every four genes, and another uncharacterized family (represented by gene B0403.1) is approximately two-thirds pseudogenic. Furthermore, over a hundred apparent pseudogenic fragments do not have any obvious homologs in the worm.
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