Literature DB >> 9736779

Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL.

K Ried1, E Rao, K Schiebel, G A Rappold.   

Abstract

We have isolated a novel gene, ASMTL (acetylserotonin methytransferase-like ), in the pseudoautosomal region (PAR1) on the human sex chromosomes. ASMTL represents a unique fusion product of two different full-length genes of different evolutionary origin and function. One part is homologous to the bacterial maf/orfE genes. The other part shows significant homology to the entire open reading frame of the previously described pseudoautosomal gene ASMT, encoding the enzyme catalysing the last step in the synthesis of melatonin. We have also detected the identity of one exon (1A) of ASMT to exon 3 in yet another pseudoautosomal gene, XE7. The data presented suggest that exon duplication and exon shuffling as well as gene fusion may represent common characteristics in the pseudoautosomal region.

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Year:  1998        PMID: 9736779     DOI: 10.1093/hmg/7.11.1771

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  16 in total

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3.  A second recombination hotspot associated with SHOX deletions.

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4.  Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome.

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Journal:  Funct Integr Genomics       Date:  2013-05-26       Impact factor: 3.410

5.  A short pseudoautosomal region in laboratory mice.

Authors:  J Perry; S Palmer; A Gabriel; A Ashworth
Journal:  Genome Res       Date:  2001-11       Impact factor: 9.043

6.  Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping.

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7.  The Human Pseudoautosomal Region (PAR): Origin, Function and Future.

Authors:  A Helena Mangs; Brian J Morris
Journal:  Curr Genomics       Date:  2007-04       Impact factor: 2.236

8.  Genomic sister-disorders of neurodevelopment: an evolutionary approach.

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9.  The Human Y Chromosome: The Biological Role of a "Functional Wasteland"

Authors:  Lluís Quintana-Murci; Marc Fellous
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10.  The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome.

Authors:  Michael A Levy; Andrew D Fernandes; Deanna C Tremblay; Claudia Seah; Nathalie G Bérubé
Journal:  BMC Genomics       Date:  2008-10-08       Impact factor: 3.969

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