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Immunobiochemical evidence for the loss of sperm specific histones during male pronucleus formation in monospermic zygotes of sea urchins

✍ Scribed by Maria Imschenetzky; Marcia Puchi; Cecilia Pimentel; Alejandra Bustos; Margarita Gonzales


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
935 KB
Volume
47
Category
Article
ISSN
0730-2312

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✦ Synopsis


To obtain information on the remodeling of sperm chromatin during male pronuclei formation, we have followed the sperm specific histones (SpH) that form the nucleosomal core by Western imunoblot analysis with policlonal antibodies directed against the core SpH. The results obtained indicate that the complete set of SpH i s absent from zygote chromatin at the beginning of the first S phase. The disappearance of SpH is not coincidental for the five histone classes: SpH4 and SpH3 are lost 5-1 5 min post insemination (p.i.), SpHZB and SpH2A disappear 20-40 min p.i., and SpH1 is progressively diminished up to 30 min p.i. This order of sperm chromatin remodeling is not affected by the inhibition of protein synthesis by emetine, indicating that the factor(s) responsible for SpH disappearance are present in unfertilized eggs. The lost SpH's are not replaced by newly synthesized CS variants, since the basic proteins synthesized de novo during male pronuclei formation are not incorporated into chromatin remaining in the cytoplasm. These newly synthesized proteins are different from the CS variants as judged by their electrophoretic migration.


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Identification of a cysteine protease re
✍ Maria Imschenetzky; Fredy Díaz; Martin Montecino; Felipe Sierra; Marcia Puchi 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 379 KB

We have identified a 60-kDa cysteine protease that is associated with chromatin in sea urchin zygotes. This enzyme was found to be present as a proenzyme in unfertilized eggs and was activated shortly after fertilization. At a pH of 7.8-8.0, found after fertilization, the enzyme degraded the five sp