Entropy based analysis of vertebrate sperm protamines sequences: evidence of potential dityrosine and cysteine-tyrosine cross-linking in sperm protamines.
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| Abstract | :  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. | 
| Year of Publication | :  2020 | 
| Journal | :  BMC genomics | 
| Volume | :  21 | 
| Issue | :  1 | 
| Number of Pages | :  277 | 
| Date Published | :  2020 | 
| URL | :  https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-020-6681-2 | 
| DOI | :  10.1186/s12864-020-6681-2 | 
| Short Title | :  BMC Genomics | 
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