Source:http://linkedlifedata.com/resource/pubmed/id/10508587
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2000-1-4
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pubmed:databankReference | |
pubmed:abstractText |
Genes evolve at different rates depending on the strength of selective pressure to maintain their function. Chromosomal position can also have an influence [1] [2]. The pseudoautosomal region (PAR) of mammalian sex chromosomes is a small region of sequence identity that is the site of an obligatory pairing and recombination event between the X and Y chromosomes during male meiosis [3] [4] [5] [6]. During female meiosis, X chromosomes can pair and recombine along their entire length. Recombination in the PAR is therefore approximately 10 times greater in male meiosis compared with female meiosis [4] [5] [6]. The gene Fxy (also known as MID1 [7]) spans the pseudoautosomal boundary (PAB) in the laboratory mouse (Mus musculus domesticus, C57BL/6) such that the 5' three exons of the gene are located on the X chromosome but the seven exons encoding the carboxy-terminal two-thirds of the protein are located within the PAR and are therefore present on both the X and Y chromosomes [8]. In humans [7] [9], the rat, and the wild mouse species Mus spretus, the gene is entirely X-unique. Here, we report that the rate of sequence divergence of the 3' end of the Fxy gene is much higher (estimated at 170-fold higher for synonymous sites) when pseudoautosomal (present on both the X and Y chromosomes) than when X-unique. Thus, chromosomal position can directly affect the rate of evolution of a gene. This finding also provides support for the suggestion that regions of the genome with a high recombination frequency, such as the PAR, may have an intrinsically elevated rate of sequence divergence.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0960-9822
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
9
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
987-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10508587-Animals,
pubmed-meshheading:10508587-Chromosome Mapping,
pubmed-meshheading:10508587-DNA, Complementary,
pubmed-meshheading:10508587-Evolution, Molecular,
pubmed-meshheading:10508587-Female,
pubmed-meshheading:10508587-Genes,
pubmed-meshheading:10508587-Humans,
pubmed-meshheading:10508587-Male,
pubmed-meshheading:10508587-Mice,
pubmed-meshheading:10508587-Mice, Inbred C57BL,
pubmed-meshheading:10508587-Muridae,
pubmed-meshheading:10508587-Phylogeny,
pubmed-meshheading:10508587-Proteins,
pubmed-meshheading:10508587-Rats,
pubmed-meshheading:10508587-Selection, Genetic,
pubmed-meshheading:10508587-Sequence Homology, Nucleic Acid,
pubmed-meshheading:10508587-Species Specificity,
pubmed-meshheading:10508587-X Chromosome,
pubmed-meshheading:10508587-Y Chromosome
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pubmed:year |
1999
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pubmed:articleTitle |
Evolutionary rate of a gene affected by chromosomal position.
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pubmed:affiliation |
Section of Gene Function and Regulation Chester Beatty Laboratories Institute of Cancer Research, 237 Fulham Road, London, SW3 6JB, UK.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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