Use of molecular beacons to verify that the serine hydroxymethyltransferase pseudogene SHMT-ps1 is unique to the order Primates 英文参考文献.docVIP
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Use of molecular beacons to verify that the serine hydroxymethyltransferase pseudogene SHMT-ps1 is unique to the order Primates 英文参考文献
/2001/2/2/research/0006.1
Research
Use of molecular beacons to verify that the serine
hydroxymethyltransferase pseudogeneSHMT-ps1 is unique to the
order Primates
Eric J Devor
Address: Molecular Genetics and Bioinformatics, Integrated DNA Technologies, Inc., 1710 Commercial Park, Coralville, IA 52241, USA.
E-mail: rdevor@
Published: 29 January 2001
Received: 22 November 2000
Revised: 20 December 2000
Accepted: 2 January 2001
GenomeBiology 2001, 2(2):research0006.1–0006.5
The electronic version of this article is the complete one and can be
found online at /2001/2/2/research/0006
? BioMed Central Ltd (Print ISSN 1465-6906; Online ISSN 1465-6914)
Abstract
Background: The serine hydroxymethyltransferase processed pseudogene SHMT-ps1 has been
suggested to be unique to the order Primates because of the failure to amplify this sequence by
PCR from genomic DNAs of any non-primate mammal species. Here, ‘molecular beacon’ probes
specific toSHMT-ps1 were used in an attempt to verify this suggestion.
Results: In a search for SHMT-ps1-specific sequences using molecular beacons across a range of
mammalian species,SHMT-ps1 was only found in primates. The molecular beacon assays also showed
thatSHMT-ps1 is present in both Old World and New World species but not among prosimians.
Conclusions: These results suggest that SHMT-ps1 originated close to the origin of the
Anthropoidea, some 40 to 50 million years ago.
Background
PCR-based analyses of evolutionary conservation of the
SHMT-ps1 nucleotide sequence suggest that the reverse tran-
scription event giving rise to SHMT-ps1 occurred after the
divergence of the order Primates from the rest of the Mam-
malia, thus making this locus a genetic marker unique to the
primates [7]. Here, this suggestion is verified using two end-
point molecular beacon assays. In addition, results presented
here further refine the time frame in which the reverse tran-
scription and re
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