Description
Mammalian spermatogenesis is associated with the transient appearance of condensed
mitochondria, a singularity of germ cells with unknown function. Using proteomic analysis,
respirometry, and electron microscopy with tomography, we studied the development of
condensed mitochondria. Condensed mitochondria arose from orthodox mitochondria
during meiosis by progressive contraction of the matrix space, which was accompanied by
an initial expansion and a subsequent reduction of the surface area of the inner membrane.
Compared to orthodox mitochondria, condensed mitochondria respired more actively,
had a higher concentration of respiratory enzymes and supercomplexes, and contained
more proteins involved in protein import and expression. After the completion of meiosis,
the abundance of condensed mitochondria declined, which coincided with the onset of the
biogenesis of acrosomes. Immuno-electron microscopy and the analysis of sub-cellular
fractions suggested that condensed mitochondria or their fragments were translocated
into the lumen of the acrosome. Thus, it seems condensed mitochondria are formed from
orthodox mitochondria by extensive transformations in order to support the formation of
the acrosomal matrix. This MassIVE dataset contains Tandem Mass Tag (TMT) peptide labeling.
[doi:10.25345/C5ST7F10D]
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: Acrosome, Cristae, Mitochondria, Spermatogenesis, Spermiogenesis
Contact
Principal Investigators:
(in alphabetical order)
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Dr. Thomas A. Neubert, New York University School of Medicine, USA
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Submitting User: |
hbromage
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Identification Results |
Proteins (Human, Remapped):
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Proteins (Reported):
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Number of distinct conditions across all analyses (original submission and reanalyses)
associated with this dataset.
Distinct condition labels are counted across all files submitted in the "Metadata" category
having a "Condition" column in this dataset.
"N/A" means no results of this type were submitted.
Number of distinct biological replicates across all analyses (original submission and reanalyses)
associated with this dataset.
Distinct replicate labels are counted across all files submitted in the "Metadata" category
having a "BioReplicate" or "Replicate" column in this dataset.
"N/A" means no results of this type were submitted.
Number of distinct technical replicates across all analyses (original submission and reanalyses)
associated with this dataset.
The technical replicate count is defined as the maximum number of times any one distinct
combination of condition and biological replicate was analyzed across all files submitted in the
"Metadata" category. In the case of fractionated experiments, only the first fraction is
considered.
"N/A" means no results of this type were submitted.
Originally identified proteins that were automatically
remapped by MassIVE to proteins in the
SwissProt
human reference database.
"N/A" means no results of this type were submitted.
Number of distinct protein accessions reported across all analyses (original submission and
reanalyses) associated with this dataset.
"N/A" means no results of this type were submitted.
Number of distinct unmodified peptide sequences reported across all analyses (original
submission and reanalyses) associated with this dataset.
"N/A" means no results of this type were submitted.
Number of distinct peptide sequences (including modified variants or peptidoforms) reported
across all analyses (original submission and reanalyses) associated with this dataset.
"N/A" means no results of this type were submitted.
Total number of peptide-spectrum matches (i.e. spectrum identifications) reported across all
analyses (original submission and reanalyses) associated with this dataset.
"N/A" means no results of this type were submitted.
Number of distinct proteins quantified across all analyses (original submission and reanalyses)
associated with this dataset.
Distinct protein accessions are counted across all files submitted in the "Statistical Analysis
of Quantified Analytes" category having a "Protein" column in this dataset.
"N/A" means no results of this type were submitted.
Number of distinct proteins found to be differentially abundant in at least one comparison
across all analyses (original submission and reanalyses) associated with this dataset.
A protein is differentially abundant if its change in abundance across conditions is found
to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated
with statistical tests for differential abundance.
Distinct protein accessions are counted across all files submitted in the "Statistical Analysis
of Quantified Analytes" category having a "Protein" column in this dataset.
"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE.
It has been imported to MassIVE for reanalysis purposes, so its spectra data here may
consist solely of processed peak lists suitable for reanalysis with most software.