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

We have isolated a novel gene, ASMTL (acetylserotonin methytransferase-likej, 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 ba...

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Bibliographic Details
Main Authors: Ried, Karin (Author) , Rao, Ercole (Author) , Schiebel, Katrin (Author) , Rappold, Gudrun (Author)
Format: Article (Journal)
Language:English
Published: 01 October 1998
In: Human molecular genetics
Year: 1998, Volume: 7, Issue: 11, Pages: 1771-1778
ISSN:1460-2083
DOI:10.1093/hmg/7.11.1771
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1093/hmg/7.11.1771
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Author Notes:K. Ried, E. Rao, K. Schiebel, G.A. Rappold
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Summary:We have isolated a novel gene, ASMTL (acetylserotonin methytransferase-likej, 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 ASMTto 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.
Item Description:Gesehen am 29.03.2021
Physical Description:Online Resource
ISSN:1460-2083
DOI:10.1093/hmg/7.11.1771