CaseDetails
Summary
Case ID
19423
Case Status
Proposal Description
As background to this work, the recovery of ancient proteins from hominid dental enamel has
previously been achieved starting from specimens up to ~2 million years old retrieved in temperate
and sub-tropical environments 1,2. The dental enamel proteome includes amelogenin, a protein that, in
humans, is expressed in two isoforms encoded in the non-recombinant regions of the
heterochromosomes, namely amelogenin X (AMELX) on the X chromosome and amelogenin Y
(AMELY) on the Y chromosome. The detection of AMELY-specific peptides allows the
straightforward assignment of the analysed dental specimen to a male individual. On the other hand,
the exclusive detection of AMELX-specific peptides is ambiguous, because it can either be
interpreted as deriving (i) from a female individual, or alternatively from (ii) a male individual whose
signal for the AMELY-specific peptides is too low to be detected, due to diagenetic degradation.
These two cases can now be discriminated with a semi-quantitative mass spectrometric approach
based on the determination of the threshold intensity of AMELX-specific peptides below which the
signal for AMELY-specific peptides is lost. This method however requires the identification of
AMELY-specific peptides in at least one dental specimen.
previously been achieved starting from specimens up to ~2 million years old retrieved in temperate
and sub-tropical environments 1,2. The dental enamel proteome includes amelogenin, a protein that, in
humans, is expressed in two isoforms encoded in the non-recombinant regions of the
heterochromosomes, namely amelogenin X (AMELX) on the X chromosome and amelogenin Y
(AMELY) on the Y chromosome. The detection of AMELY-specific peptides allows the
straightforward assignment of the analysed dental specimen to a male individual. On the other hand,
the exclusive detection of AMELX-specific peptides is ambiguous, because it can either be
interpreted as deriving (i) from a female individual, or alternatively from (ii) a male individual whose
signal for the AMELY-specific peptides is too low to be detected, due to diagenetic degradation.
These two cases can now be discriminated with a semi-quantitative mass spectrometric approach
based on the determination of the threshold intensity of AMELX-specific peptides below which the
signal for AMELY-specific peptides is lost. This method however requires the identification of
AMELY-specific peptides in at least one dental specimen.
Inventory Reference
Post date
13/03/2023 - 12:14
Last modified
21/10/2023 - 13:34
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Decisions, Comments + Permits
Decision Date | Type | |
---|---|---|
Permit | Access Document | |
Letter | Access Document |