Javascript must be enabled to continue!
The sperm nuclear matrix is required for paternal DNA replication
View through CrossRef
AbstractThe mammalian sperm nucleus provides an excellent model for studying the relationship between the formation of nuclear structure and the initiation of DNA replication. We previously demonstrated that mammalian sperm nuclei contain a nuclear matrix that organizes the DNA into loop domains in a manner similar to that of somatic cells. In this study, we tested the minimal components of the sperm nucleus that are necessary for the formation of the male pronucleus and for the initiation of DNA synthesis. We extracted mouse sperm nuclei with high salt and dithiothreitol to remove the protamines in order to form nuclear halos. These were then treated with either restriction endonucleases to release the DNA not directly associated with the nuclear matrix or with DNAse I to digest all the DNA. The treated sperm nuclei were injected into oocytes, and the paternal pronuclear formation and DNA synthesis was monitored. We found that restriction digested sperm nuclear halos were capable of forming paternal pronuclei and initiating DNA synthesis. However, when isolated mouse sperm DNA or sperm DNA reconstituted with the nuclear matrices were injected into oocytes, no paternal pronuclear formation or DNA synthesis was observed. These data suggest that the in situ nuclear matrix attachment organization of sperm DNA is required for mouse paternal pronuclear DNA synthesis. J. Cell. Biochem. 102: 680–688, 2007. © 2007 Wiley‐Liss, Inc.
Title: The sperm nuclear matrix is required for paternal DNA replication
Description:
AbstractThe mammalian sperm nucleus provides an excellent model for studying the relationship between the formation of nuclear structure and the initiation of DNA replication.
We previously demonstrated that mammalian sperm nuclei contain a nuclear matrix that organizes the DNA into loop domains in a manner similar to that of somatic cells.
In this study, we tested the minimal components of the sperm nucleus that are necessary for the formation of the male pronucleus and for the initiation of DNA synthesis.
We extracted mouse sperm nuclei with high salt and dithiothreitol to remove the protamines in order to form nuclear halos.
These were then treated with either restriction endonucleases to release the DNA not directly associated with the nuclear matrix or with DNAse I to digest all the DNA.
The treated sperm nuclei were injected into oocytes, and the paternal pronuclear formation and DNA synthesis was monitored.
We found that restriction digested sperm nuclear halos were capable of forming paternal pronuclei and initiating DNA synthesis.
However, when isolated mouse sperm DNA or sperm DNA reconstituted with the nuclear matrices were injected into oocytes, no paternal pronuclear formation or DNA synthesis was observed.
These data suggest that the in situ nuclear matrix attachment organization of sperm DNA is required for mouse paternal pronuclear DNA synthesis.
J.
Cell.
Biochem.
102: 680–688, 2007.
© 2007 Wiley‐Liss, Inc.
Related Results
P-046 Effect of different sperm chromatin dispersion type on IVF/ICSI outcome and offspring profile
P-046 Effect of different sperm chromatin dispersion type on IVF/ICSI outcome and offspring profile
Abstract
Study question
Whether the percentage of different sperm chromatin dispersion type are associated with the IVF/ICSI out...
P–025 Sperm selection using a modified “swim up” technique in absence of sperm centrifugation improve sperm DNA fragmentation and decreases miscarriage rate
P–025 Sperm selection using a modified “swim up” technique in absence of sperm centrifugation improve sperm DNA fragmentation and decreases miscarriage rate
Abstract
Study question
Is it useful to avoid sperm centrifugation in laboratory routine work to improve sperm quality and repro...
P–069 microfluidic sperm sorting vs density gradient to yield sperm with reduced DFI for patients undergoing IVF-ICSI
P–069 microfluidic sperm sorting vs density gradient to yield sperm with reduced DFI for patients undergoing IVF-ICSI
Abstract
Study question
To compare the effect of sperm preparation methods on the DFI of semen sample for patients undergoing IC...
P–103 Novel sperm preparation techniques compared with conventional preparation method
P–103 Novel sperm preparation techniques compared with conventional preparation method
Abstract
Study question
Which sperm preparation technique separate the best quality sperm?
...
Optimization of the TLR7/8 Activation-Based Sorting System for Goat Sperm
Optimization of the TLR7/8 Activation-Based Sorting System for Goat Sperm
Background:Current research indicates that the immunological separation method based on differentially expressed proteins in X- and Y-chromosome-bearing sperm represents a novel ap...
Sperm DNA damage in men with severe asthenozoospermia
Sperm DNA damage in men with severe asthenozoospermia
Background. Sperm motility is a fundamental factor for sperm penetration into the oocyte and fertilization. According to the World Health Organization (WHO) 2021, less than 42% of ...
Sperm Quality Assessment of White Shrimp (Litopenaeus Vannamei) Broodstock using Comet Assay
Sperm Quality Assessment of White Shrimp (Litopenaeus Vannamei) Broodstock using Comet Assay
The quality of sperms is considered one of the factors determining fertilization success of white shrimp, Litopenaeus vannamei. Generally, conventional methods such as sperm count ...
P-072 Fresh testicular sperm seems to yield more fertilization abnormalities and early pregnancy loss than frozen testicular sperm
P-072 Fresh testicular sperm seems to yield more fertilization abnormalities and early pregnancy loss than frozen testicular sperm
Abstract
Study question
How do ICSI outcomes using fresh testicular sperm, compare to those using frozen samples cryopreserved f...

