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Entropy based analysis of vertebrate sperm protamines sequences: evidence of potential dityrosine and cysteine-tyrosine cross-linking in sperm protamines
- Source :
- BMC Genomics, BMC Genomics, Vol 21, Iss 1, Pp 1-10 (2020)
- Publication Year :
- 2020
- Publisher :
- Springer Science and Business Media LLC, 2020.
-
Abstract
- Background Spermatogenesis is the process by which germ cells develop into spermatozoa in the testis. Sperm protamines are small, arginine-rich nuclear proteins which replace somatic histones during spermatogenesis, allowing a hypercondensed DNA state that leads to a smaller nucleus and facilitating sperm head formation. In eutherian mammals, the protamine-DNA complex is achieved through a combination of intra- and intermolecular cysteine cross-linking and possibly histidine-cysteine zinc ion binding. Most metatherian sperm protamines lack cysteine but perform the same function. This lack of dicysteine cross-linking has made the mechanism behind metatherian protamines folding unclear. Results Protamine sequences from UniProt’s databases were pulled down and sorted into homologous groups. Multiple sequence alignments were then generated and a gap weighted relative entropy score calculated for each position. For the eutherian alignments, the cysteine containing positions were the most highly conserved. For the metatherian alignment, the tyrosine containing positions were the most highly conserved and corresponded to the cysteine positions in the eutherian alignment. Conclusions High conservation indicates likely functionally/structurally important residues at these positions in the metatherian protamines and the correspondence with cysteine positions within the eutherian alignment implies a similarity in function. One possible explanation is that the metatherian protamine structure relies upon dityrosine cross-linking between these highly conserved tyrosines. Also, the human protamine P1 sequence has a tyrosine substitution in a position expecting eutherian dicysteine cross-linking. Similarly, some members of the metatherian Planigales genus contain cysteine substitutions in positions expecting plausible metatherian dityrosine cross-linking. Rare cysteine-tyrosine cross-linking could explain both observations.
- Subjects :
- Male
endocrine system
Protein Folding
lcsh:QH426-470
lcsh:Biotechnology
Sperm Chromatin
Entropy
030303 biophysics
Protamine
03 medical and health sciences
chemistry.chemical_compound
lcsh:TP248.13-248.65
Cross-Linking
Genetics
Animals
Amino Acid Sequence
Cysteine
Protamines
Relative Entropy
Tyrosine
Nuclear protein
Zinc ion binding
Conserved Sequence
030304 developmental biology
0303 health sciences
Binding Sites
biology
Eutheria
Computational Biology
DNA
Spermatozoa
Sperm
Cell biology
lcsh:Genetics
Histone
chemistry
biology.protein
Sequence Alignment
Research Article
Protein Binding
Biotechnology
Subjects
Details
- ISSN :
- 14712164
- Volume :
- 21
- Database :
- OpenAIRE
- Journal :
- BMC Genomics
- Accession number :
- edsair.doi.dedup.....d263a0a7b2ce6d7a0267f6d66ed3d018
- Full Text :
- https://doi.org/10.1186/s12864-020-6681-2