ArticleProceedings of the National Academy of Sciences of the United States of America1994
Evidence that most human Alu sequences were inserted in a process that ceased about 30 million years ago.
Article in Proceedings of the National Academy of Sciences of the United States of America, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.
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Who cites it
32 citing papers in PubMed.
- A transposable element prevents severe hemophilia B and provides insights into the evolution of new- and old world primates.PloS one · 2024Article
- Alu RNA fold links splicing with signal recognition particle proteins.Nucleic acids research · 2023Article
- Evolutionary dynamics of selfish DNA explains the abundance distribution of genomic subsequences.Scientific reports · 2016Article
- Tangram: a comprehensive toolbox for mobile element insertion detection.BMC genomics · 2014Article
- Inference of transposable element ancestry.PLoS genetics · 2014Article
- Human transposon tectonics.Cell · 2012Review
- LINEs and SINEs of primate evolution.Evolutionary anthropology · 2010Article
- Population bottlenecks as a potential major shaping force of human genome architecture.PLoS genetics · 2007Article
- Article
- Under the genomic radar: the stealth model of Alu amplification.Genome research · 2005Article
- Genomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineages.Nucleic acids research · 2005Article
- The association of Alu repeats with the generation of potential AU-rich elements (ARE) at 3' untranslated regions.BMC genomics · 2004Article
- Comparative analysis of Alu insertion sequences in the APP 5' flanking region in humans and other primates.Journal of molecular evolution · 2004Article
- Majority of divergence between closely related DNA samples is due to indels.Proceedings of the National Academy of Sciences of the United States of America · 2003Article
- Whole-genome screening indicates a possible burst of formation of processed pseudogenes and Alu repeats by particular L1 subfamilies in ancestral primates.Genome biology · 2003Article
- HERV-K(OLD): ancestor sequences of the human endogenous retrovirus family HERV-K(HML-2).Journal of virology · 2001Article
- Transcriptional and translational mechanisms of cytochrome b5 reductase isoenzyme generation in humans.The Biochemical journal · 2001Article
- Recent, extensive, and preferential insertion of members of the miniature inverted-repeat transposable element family Heartbreaker into genic regions of maize.Proceedings of the National Academy of Sciences of the United States of America · 2000Article
- Structure and upstream region characterization of the human gene encoding rod photoreceptor cGMP phosphodiesterase alpha-subunit.Journal of molecular neuroscience : MN · 1998Article
- The decline in human Alu retroposition was accompanied by an asymmetric decrease in SRP9/14 binding to dimeric Alu RNA and increased expression of small cytoplasmic Alu RNA.Molecular and cellular biology · 1997Article
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1 author.
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Abstract
The primate Alu interspersed repeats can be subdivided into classes on the basis of shared nucleotides at a set of diagnostic positions. Each of the classes of Alu sequences is apparently the result of past retrotransposition of transcripts of highly conserved class-specific source genes that differed from each other at the diagnostic positions. The nucleotides at the majority of positions are identical among the source genes and therefore were identical among all of the Alu sequences at the time of their insertion. These CONSBI (conserved before insertion) positions are useful because the changes that have occurred after insertion are recognizable and the divergence resulting from nucleotide substitutions, insertions, and deletions is informative. The divergence of Alu sequences at the CONSBI positions is a measure of the time since a class was inserted. The greatest majority of Alu sequences are in one class (identified as class II), and it is particularly suitable for such examination, since nearly full-length sequences are now known for nearly a thousand members of this class. The average divergence of class II members indicates that the class has an average age of about 40 million years. The distribution in divergence of class II accurately fits a sum of two Poisson distributions. The implication is that class II Alu sequences were derived from two massive past events of insertion of many Alu sequences. In this model the younger subset of class II sequences (corresponding to about 300,000 copies in the genome) has an average divergence of 5% at CONSBI positions. The older set of class II sequences (corresponding to about 150,000 genomic copies) has a 9% average divergence. Based on the drift rate of primate DNA sequences, the events of insertion probably occurred 30-50 million years ago. The goodness of the fit to the Poisson distribution indicates that no significant number of members of class II have been inserted since 30 million years ago.
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