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
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| Journal | :
BMC genomics
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| Volume | :
21
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| Issue | :
1
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| Number of Pages | :
277
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| Date Published | :
2020
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| URL | :
https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-020-6681-2
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| DOI | :
10.1186/s12864-020-6681-2
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| Short Title | :
BMC Genomics
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