Deficiency in mouse Y chromosome long arm gene complement is associated with sperm DNA damage
- Yasuhiro Yamauchi†1,
- Jonathan M Riel†1,
- Zoia Stoytcheva1,
- Paul S Burgoyne2 and
- Monika A Ward1Email author
© Yamuachi et al.; licensee BioMed Central Ltd. 2010
Received: 13 April 2010
Accepted: 23 June 2010
Published: 23 June 2010
Mice with severe non-PAR Y chromosome long arm (NPYq) deficiencies are infertile in vivo and in vitro. We have previously shown that sperm from these males, although having grossly malformed heads, were able to fertilize oocytes via intracytoplasmic sperm injection (ICSI) and yield live offspring. However, in continuing ICSI trials we noted a reduced efficiency when cryopreserved sperm were used and with epididymal sperm as compared to testicular sperm. In the present study we tested if NPYq deficiency is associated with sperm DNA damage - a known cause of poor ICSI success.
We observed that epididymal sperm from mice with severe NPYq deficiency (that is, deletion of nine-tenths or the entire NPYq gene complement) are impaired in oocyte activation ability following ICSI and there is an increased incidence of oocyte arrest and paternal chromosome breaks. Comet assays revealed increased DNA damage in both epididymal and testicular sperm from these mice, with epididymal sperm more severely affected. In all mice the level of DNA damage was increased by freezing. Epididymal sperm from mice with severe NPYq deficiencies also suffered from impaired membrane integrity and abnormal chromatin condensation and suboptimal chromatin protamination. It is therefore likely that the increased DNA damage associated with NPYq deficiency is a consequence of disturbed chromatin remodeling.
This study provides the first evidence of DNA damage in sperm from mice with NPYq deficiencies and indicates that NPYq-encoded gene/s may play a role in processes regulating chromatin remodeling and thus in maintaining DNA integrity in sperm.
Intracytoplasmic sperm injection with cryopreserved epididymal sperm from NPYq-2 males
Number of oocytes injected
Number of oocytes survived (%)a
Number of oocytes activated (%)b, c
Number of oocytes cleaved (%)b
Number of two-cell embryos transferred (number of surrogates)
Number of pregnant surrogates
Number of fetuses
Epididymal sperm from males with NPYq deficiencies are less efficient in oocyte activation after ICSI than testicular sperm
To test for sperm origin or freezing effects on ICSI outcome, injections were carried out with fresh or frozen epididymal sperm, and fresh or frozen testicular sperm. Two males were sampled for each NPY-deficient and the matched control genotypes (see Materials and methods for mouse genotype details).
A caveat to this initial analysis is that there were indications of significant inter-male variability, particularly with respect to the two NPYq-2 males. We therefore carried out 'within genotype' comparisons of epididymal and testicular sperm, both fresh and frozen, keeping the individual male data separate, and testing for significant differences using Mantel-Haenszel chi square analysis, which takes account of male to male variation. The control genotypes XYRIII and XY Tdym1 Sry did not show any significant differences between epididymal and testicular sperm, whether fresh or frozen, in their ability to activate oocytes. As would be expected from the NPYq-deficient versus control comparisons, there was a significant reduction in the oocyte activation efficiency with fresh epididymal sperm as compared to fresh testicular sperm, and with frozen epididymal sperm relative to frozen testicular sperm in NPYq-2 and 9/10NPYq- (Figure 1a). In contrast, the fresh epididymal sperm from 2/3NPYq- gave a significantly higher level of activation than fresh testicular sperm or frozen epididymal sperm.
The above analyses point to NPYq deficiency being a cause of impaired epididymal sperm function, with these effects being proportional to the extent of NPYq gene loss. In the light of this we decided to carry out a single analysis of all the NPYq-deficient male data by ANOVA, with genotype, sperm source (testis or epididymis) and sperm status (fresh or frozen) as factors; an identical analysis was carried out on the two control genotypes for comparison. For these ANOVAs, oocyte activation percentages for individual males were transformed into angles. No significant differences for the three factors were detected among the controls. In contrast, the analysis of the NPYq-deficient male data revealed significant effects of genotype (progressively reduced activation with increasing NPYq-deficiency; P = 0.036), sperm source (less activation with epididymal sperm than testicular sperm; P = 0.020), and a genotype/source interaction (epididymal sperm more affected by NPYq-deficiency than testicular sperm; P = 0.038; Figure 1b). Thus, these ANOVA analyses confirm the conclusions from the prior analyses.
We conclude that there is a reduction in oocyte activation that increases with the extent of NPYq deficiency, and this effect of NPYq deficiency is largely confined to epididymal sperm.
NPYq deficiency is associated with sperm DNA damage
Poor activation rates can be circumvented by artificial activation but we have found that even with artificial activation ICSI success rates remained very low with frozen epididymal sperm from NPYq-2 males (Table 1), so we suspected that DNA damage may be an important additional factor. We therefore performed comet assays on epididymal and testicular sperm to directly test for DNA damage.
Testicular sperm samples for comet assay were prepared in the same manner as for ICSI so they included other testicular cell types that are not present in the epididymal sperm samples. To test if the presence of these other cell types affects comet assay results, experiments were performed in which a portion of both epididymal and fresh testicular cell suspensions were sonicated under conditions that eliminate these sonication-sensitive cells; comet assays were then performed on non-sonicated and matched sonicated samples, both before and after freezing. Two males of each of the genotypes XYRIII, XY Tdym1 Sry, and 2/3NPYq- were analyzed; 100 sperm comet tail lengths were measured from each male. The comet tail length data were analyzed by ANOVA with sonication status (sonicated or non-sonicated), genotype, sperm source (testis or epididymis) and sperm status (fresh or frozen) as factors. There were no significant effects of sonication so the fuller analysis including all the NPYq-deficient and control genotypes was therefore carried out without sonication.
We then compared each NPYq-deficient genotype with its matched control. There were no significant differences between 2/3NPYq- and the XYRIII control, but the two remaining NPYq-deficient genotypes had significantly increased sperm comet tail lengths relative to their controls (Figure 2c). Analysis of the three NPYq-deficient genotypes in a single ANOVA showed (as in controls) a significant increase of comet tail length in response to freezing (P = 0.0084; Figure 2a); in contrast to controls there was no significant increase in comet tail length in testicular sperm as compared to epididymal sperm (Figure 2b). Indeed, when the effect of sperm source was compared in analyses within each NPYq-deficient genotype, comet tails were significantly longer in epididymal sperm as compared to testicular sperm from NPYq-2 (P = 0.0034), and this resulted in a highly significant genotype/sperm source interaction (P = 0.0004) when NPYq-2 was compared with its matched XYRIII control.
The comet data show that freezing increases DNA damage across all genotypes, that there is an increase in DNA damage relative to controls when the NPYq-deficiency exceeds that of 2/3NPYq-, and that epididymal sperm from mice with severe NPYq-deficiency are more susceptible to DNA damage than testicular sperm. We conclude that severe NPYq deficiency leads to DNA damage that is particularly marked in frozen epididymal sperm, and that this is likely to be the major factor underlying the very poor ICSI outcome using frozen epididymal sperm from NPYq-2 males.
NPYq deficiencies yield a high incidence of oocyte arrest and paternal chromosome breaks after ICSI
When collecting the ICSI activation data, we also collected data on the incidence of early post-fertilization oocyte arrest and of chromosome breakage in the paternal chromosome complements of zygotes, since both are known consequences of sperm DNA damage [13, 14].
Based on the ANOVA analysis we conclude that in controls the freezing of testicular sperm leads to significant chromosome damage, and that severe NPYq deficiency leads to a marked increase in chromosome damage in response to sperm freezing, with testicular and epididymal sperm now being affected.
Comparison of sperm comet and chromosome aberration data indicates that testicular sperm freezing impairs sperm DNA damage repair in the oocyte
There is substantial evidence showing that oocytes have DNA repair machinery present at fertilization that enables DNA damage in the sperm nucleus to be repaired . The chromosome aberrations present in fertilized oocytes are therefore a manifestation of prior DNA damage that cannot be repaired by the oocyte. For six of the males in the present study the same sperm samples were used for the sperm comet and oocyte paternal chromosome complement analyses, so a direct comparison of these sets of data should highlight those factors that lead to irreparable DNA damage.
The six males for which both sets of data are available are XYRIII (n = 1), 2/3NPYq- (n = 2), 9/10NPYq- (n = 1) and NPYq-2 (n = 2). Because 2/3NPYq- males (with moderate NPYq deficiency) do not manifest any significant differences from XYRIII in either assay, we treated the first three males as one group (group 1, G1). The 9/10NPYq- and NPYq-2 males (severe NPYq deficiency) constituted the second group (group 2, G2), which differed markedly from their controls in both assays. The two groups were first compared by ANOVA. For sperm comet tail length there was a 38% increase as a consequence of severe NPYq deficiency (P < 0.000001); epididymal sperm were preferentially affected in G2 whereas in G1 it was the testicular sperm that had the longer sperm comet tails (group/sperm source interaction, P = 0.0032). For chromosome aberration rate there was an almost six-fold increase as a consequence of the NPYq deficiency (P = 0.000013); sperm from G2 males were much more sensitive to freezing than those from G1, resulting in a significant group/sperm status interaction (P = 0.00070).
Sperm from males with NPYq deficiencies have impaired membrane integrity and abnormal chromatin condensation as shown by electron microscopy analysis
Transmission electron microscopy was used to determine membrane integrity and appearance of chromatin in epididymal sperm from mice with NPYq deficiencies. Three males per genotype were examined (except for 9/10NPYq-, for which only two males were tested) and 100 sperm heads were scored per male.
When examining chromatin condensation we categorized sperm into three categories: those with properly condensed (C), slightly decondensed (SLD) and severely decondensed (SVD) chromatin (Figure 9). All controls had the vast majority of sperm with properly condensed chromatin (>90%). In 2/3NPYq- males, sperm with properly condensed chromatin predominated (66%) and less than 10% had severely decondensed chromatin. In 9/10NPYq- and NPYq-2 males more than half of sperm had decondensed chromatin (approximately 57% and approximately 79%, respectively). All NPYq-deficient genotypes had fewer sperm with properly condensed chromatin and more sperm with slightly and severely decondensed sperm than their respective controls.
When membrane integrity and chromatin condensation status were compared, the test for linear trend in proportions  confirmed a significant correlation between the maintenance of sperm membrane integrity and proper chromatin condensation (P < 0.001).
Overall, the data show that mice with NPYq deficiencies exhibit membrane damage and abnormal chromatin condensation in sperm, which increases in parallel with the level of NPYq gene loss.
Sperm from males with NPYq deficiencies have impaired protamine processing
Western blot analysis of protamines in mice with NPYq deficiencies
Mean band intensityb (±SEM) representing mature protamine forms
Hub2B (protamine 2)
Mean band intensityb (±SEM) representing immature protamine 2 (PreP2)
2/3NPYq- (n = 7)
141.9 ± 4.6
125.3 ± 4.6
XYRIII (n = 6)
138.2 ± 5.0
124.9 ± 5.0
9/10NPYq- (n = 7)
82.5 ± 4.8*
43.5 ± 0.3***
9/10NPYq- (n = 5)
89.2 ± 4.5**
XY Tdym1 Sry (n = 6)
131.0 ± 5.2
49.3 ± 0.3
XY Tdym1 Sry (n = 4)
53.8 ± 5.0
NPYq-2 (n = 3)
22.1 ± 16.2
20.8 ± 6.6
XYRIII (n = 3)
76.0 ± 16.2
36.9 ± 6.6
In summary, the data indicate that mice with severe NPYq deficiencies have impaired sperm chromatin protamination leading to an increase in premature protamine forms and a decrease in mature protamine forms in epididymal sperm.
The aim of the present study was to provide an explanation for the very poor ICSI success when using frozen epididymal sperm from mice with severe NPYq deficiency. The results show that the major underlying cause is an increase in DNA damage that particularly affects epididymal sperm, and that is further increased by sperm freezing. This DNA damage included damage that was not reparable by the DNA repair machinery present in the oocyte, resulting in a marked increase in chromosome aberrations in the paternal chromosome complement following ICSI.
What is the origin of the increased sperm DNA damage in severely NPYq-deficient mice that is already detected in testicular sperm and has increased markedly by the time the sperm have reached the cauda epididymis? The origin of sperm DNA damage is a subject of substantial research and much debate. Aitken et al. [17, 18] have proposed a two step model in which sperm exiting the testis with chromatin remodeling defects, such as incomplete protamination, histone retention and poor compaction, subsequently acquire membrane and DNA damage as they transit the epididymis. Several proposed, not mutually exclusive causes of this DNA damage include direct damage by reactive oxygen species [17, 19] and the action of endonucleases present either within the sperm or in epididymal fluid [13, 20–22]. However, there is also evidence that damaged spermatozoa can be selectively removed during epididymal transit [23, 24], so the level of DNA damage detected in sperm from the cauda epididymis depends on the balance between the generation of DNA damage and the removal of sperm with DNA damage during epididymal transit. Thiol-cross linking, which takes place during epididymal maturation [25–27], increases overall chromatin compaction. If sperm exiting testes already have some chromatin defect, epididymal maturation may be impaired or may not take place.
In the case of severely NPYq-deficient mice, the primary defect must arise during spermiogenesis since this is when the NPYq-encoded genes are expressed in normal mice [3, 5, 28]. In keeping with the two step model for the generation of DNA damage in epididymal sperm , we have found that epididymal sperm from NPYq deficient mice have defective protamination and chromatin compaction, with associated membrane damage. However, testicular sperm from these mice already have elevated levels of DNA double-strand breaks (DSBs) as detected by the comet assay. Transient DSBs are generated by topoisomerase TOP2B during normal sperm chromatin remodeling and it has been suggested that inefficient repair of these breaks may occur in the context of disturbed protamination [29, 30].
The exact mechanistic link between NPYq deficiency and the chromatin changes is difficult to determine because of the major transcriptional changes in spermatids that are associated with NPYq deletions. More than 200 genes were found to be differentially expressed in mice with NPYq deficiencies, as compared to wild-type controls, the most striking change being the over-expression of sex chromosome linked genes; among the misregulated genes are some that are implicated in chromatin remodeling during spermiogenesis (NPYp-linked H2al2y, X-linked H2al1 and Cypt, and autosomal Hist1h3, Hist1h4, Chaf1b and Speer) [28, 31]. Given the extent of this transcriptional regulation, it is perhaps unsurprising that there are also changes in the pattern of spermatid chromatin modifications . The majority of these genes are also misregulated in mice with a specific small interfering RNA-mediated disruption of the function of the multi-copy NPYq gene Sly. These mice are near sterile and recapitulate most of the features associated with severe NPYq deficiency, including altered patterns of spermatid chromatin modifications, thus demonstrating that this multi-copy NPYq gene plays a key role in regulating spermiogenic gene expression . No homologues of Sly or the other multi-copy mouse NPYq genes have been identified on the human Y chromosome. Nevertheless, multi-copy testis expressed genes are a feature of the human Y [33, 34] and the multi-copy testis specific gene RBMY has a multi-copy homologue (Rbmy) on the mouse Y short arm . Thus, the two species have in common the fact that genes with a presumed or demonstrated spermatogenic role are often amplified on the Y.
DSBs are extremely hazardous lesions that must be repaired before cell division occurs if cell death is to be avoided. It is well established that oocytes have the DNA damage repair machinery in place to repair DSBs once the sperm chromatin begins to decondense as it is deprotaminated [15, 36–39]; this initial repair utilizes non-homologous end joining (NHEJ) to re-ligate the broken ends  and our data suggest this mechanism is sufficient to deal with any DSBs in epididymal sperm from controls, even when the numbers are increased by freezing. However, with fresh epididymal sperm from NPYq-deficient mice there is an elevation in the chromosome aberration rate manifested as broken chromosomes and chromosome rearrangements; with freezing this is further increased, leading to elevated levels of chromosome aberrations also in testicular sperm from control and NPYq-deficient males. These chromosome aberrations are manifestations of unrepaired DSBs. Chromosome rearrangements occur when the 'wrong' DNA ends are ligated, and constitute evidence that the original broken ends have not been maintained in juxtaposition; instead there has been a chance juxtaposition of non-matching ends that are then ligated by NHEJ. The chromosome breaks almost certainly represent the separation of broken DNA ends without the chance finding of an alternative partner. How broken DNA ends might be held in juxtaposition in the protaminated chromatin of the sperm head is not known; nevertheless, the data we have obtained suggest that with incompletely protaminated DNA, as in testicular sperm and in epididymal sperm from NPYq deficient mice, the nuclear matrix/protein scaffold holding the DNA ends together is susceptible to disruption by freezing.
What are the broader implications of the present findings? ICSI is widely used to treat human male infertility due to oligozoospermia or teratozoospermia that is usually associated with sperm defects, such as incomplete protamination and incomplete compaction of the chromatin  (reviewed in [41, 42]). Thus, the severely NPYq-deficient mice studied here are a useful mouse model for assessing the consequences of these defects for the offspring. It is also important to consider the implications of the additional DNA damage that arises as a consequence of freezing in the NPYq-deficient mice as well as in the controls. With freezing and NPYq deficiency, almost none of the embryos transferred reached term; this is unsurprising given the level of chromosome breaks and rearrangements generated, which would be expected to cause early embryonic lethality. This raises a number of issues as to how to maximize ICSI success and how to minimize mutational load in the offspring. In the context of ICSI success it seems clear that in situations where there is increasing DNA damage during epididymal transit, as is the case with NPYq deficiency, it is better to use testicular sperm; however, freezing should be avoided. Improved ICSI success with testicular as compared to epididymal sperm has previously been reported for mice heterozygous for two different but semi-identical translocations  and in mice deficient for transition proteins [11, 44], as well as in infertile men with sperm DNA damage . A caveat is that in the present study sperm freezing was done without cryoprotectant, but with the method developed to keep DNA damage to a level comparable to freezing with cryprotectant [46, 47]. Indeed, substantial freezing-induced DNA damage has been reported even with mouse sperm frozen with cryoprotectant  and with cryopreserved human sperm [49–51].
As to mutational load, NHEJ is inevitably mutagenic even when the correct partners are re-ligated , so it is expected that the mutational load will increase as the DNA damage increases; this is supported by a recent study of offspring generated by ICSI using frozen-thawed mouse sperm . It has also been argued that disturbances of chromatin remodeling can generate 'epi-mutations' that can contribute to the mutational load across generations . Aside from the implications for treating human infertility by ICSI, our findings raise questions as to the mutational load associated with the use of cryopreserved sperm in general. With the extensive single nucleotide polymorphism mapping panels now available that provide sequence-based, genome-wide markers, it should be possible to screen for DNA sequence changes arising as a consequence of sperm freezing.
We provide the first evidence on sperm DNA damage in conjunction with deletions of the Y chromosome long arm (NPYq) in mice, with support for the underlying mechanism. NPYq-deficient mice serve as a model for human infertility cases due to Y chromosome deletions and/or cases associated with sperm DNA damage and abnormal sperm chromatin compaction. In addition to demonstrating the involvement of NPYq-encoded genes in regulating chromatin remodeling during spermiogenesis, the study also provides important insights into the regulation of sperm DNA integrity after they are released from the testis, in the epididymis and in the oocyte after fertilization. In the context of other recently published work, our study points to there being an increased mutational load across generations as a consequence of assisted reproduction with sperm resulting from defective chromatin compaction during spermiogenesis or sperm subjected to cryopreservation.
Materials and methods
Mineral oil was purchased from Squibb and Sons (Princeton, NJ, USA); pregnant mares' serum gonadotrophin (eCG) and human chorionic gonadotrophin (hCG) from Calbiochem (San Diego, CA, USA). All other chemicals were obtained from Sigma Chemical Co. (St Louis, MO, USA) unless otherwise stated.
Six- to twelve-week-old B6D2F1 (C57BL/6J × DBA/2) females (NCI, Raleigh, NC, USA) were used as oocyte donors for ICSI. The mice of interest in this study were three mutant mice with progressive NPYq deficiency: XYRIIIqdel (subsequently called 2/3NPYq) - these males have a RIII strain-derived Y chromosome with a deletion removing approximately two-thirds of NPYq; XY Tdym1 qdelSry (subsequently called 9/10NPYq-) - these males have a 129 strain-derived Y chromosome with an 11-kb deletion removing the testis determinant Sry  that is complemented by an autosomally located Sry transgene , together with a deletion removing approximately nine-tenths of NPYq ; and XY*XSxra (subsequently called NPYq-2)  - in these males the only Y specific material is provided by the YRIII short arm derived sex reversal factor Sxra that is attached distal to the PAR of the Y*X chromosome. The Y*X chromosome is an X chromosome with a very large deletion removing most of the X-specific region but leaving an intact PAR and X PAR boundary, together with the X centromere . NPYq-2 males lack the entire Y-specific (non-PAR) gene content of Yq in addition to a reduction in copies of Rbmy on Yp. The control for 2/3NPYq- and NPYq-2 mice is XYRIII, and for 9/10NPYq- is XY Tdym1 Sry mice, which carry the same Y chromosome on which the deletion variant arose. All mice were produced 'in-house' by either breeding or assisted reproduction, and were on a predominantly C57BL/6 genetic background (more than six generation backcross from MF1 for all males except for NPYq-2, which were either 62.5% or 81.25% C57BL/6). The mice were maintained in accordance with the NCR 'Guide for Care and Use of Laboratory Animals' in rooms at 22°C with 14 h light/10 h dark, and fed ad libitum.
Gamete collection and embryo culture
Oocyte collection and subsequent oocyte manipulation, including microinjections, were done in HEPES-buffered CZB medium (HEPES-CZB) , with subsequent culture in CZB with an atmosphere of 5% CO2 in air . To obtain testicular sperm a portion of testis was cut off and minced in ETBS (an EGTA Tris-HCl-buffered solution consisting of 50 mM EGTA, 50 mM NaCl, and 10 mM Tris-HCl buffer, pH 8.2-8.5 ) or HEPES-CZB to release spermatogenic cells. To obtain epididymal sperm the contents of the caudae epididymides were expressed with needles and placed in HEPES-CZB, ETBS or phosphate-buffered saline. Spermatozoa were allowed to disperse for 2 to 3 minutes at room temperature. The samples of testicular or epididymal cell suspension were used for ICSI, comet assay, preparation for transmission electron microscope (TEM) analysis or sperm nuclear protein isolation immediately after dispersion, or were subjected to freezing. In some cases epididymal and testicular samples were sonicated before freezing and/or comet assay (65 output, 10 pulses 1 s each). After sonication the cell suspension was layered over a two-layer (1.8 to 2.2 M) sucrose gradient and centrifuged (400 g, 20 minutes). The pellet was resuspended in HEPES-CZB or ETBS, and checked under the light microscope to confirm that only sonication-resistant cells (sperm and elongated spermatids) were present.
Epididymal and testicular sperm freezing
Aliquots of 10 μl epididymal sperm or testicular cell suspension in ETBS were loaded in 0.25 ml straws (Edwards Innovations, Spring Valley, VA, USA). Each straw was sealed with Critoseal (Oxford Labware, St Louis, MO, USA) and placed in a plastic holder floating on the surface of the liquid nitrogen for 10 minutes before immersion. For thawing, the straws were removed from the storage container and immersed in a water bath at 37°C for 10 minutes and the contents expressed into a Petri dish. Spermatozoa were used immediately for ICSI or other analyses.
Intracytoplasmic sperm injection
ICSI was carried out as previously described  within 1 to 2 h from oocyte collection and with live sperm randomly chosen for the injections. Sperm-injected oocytes were transferred into CZB medium and cultured at 37°C. The survival of ICSI oocytes was scored 1 to 2 h after the commencement of culture. The activation of ICSI oocytes was scored 6 h after the commencement of culture; the oocytes with two well-developed pronuclei and extruded second polar body were considered activated. The number of two-cell embryos ('fertilized') was recorded after 24 h in culture.
Chromosome preparation and analysis were performed as previously described [13, 14]. The Y chromosome of 9/10NPYq- males and the Y*X chromosome of NPYq-2 males are minute and the latter males also generate some sperm lacking a sex chromosome [7, 8]. Therefore, for these two genotypes the presence of one small variant and/or lack of one chromosome in the paternal chromosome complement were considered normal. For control males the chromosomes of a spermatozoon were considered normal when an oocyte contained 40 normal metaphase chromosomes, 20 maternal and 20 paternal. It was not always possible to distinguish between chromosomes of paternal and maternal origin. However, since oocyte chromosomes rarely show structural aberrations at first cleavage metaphase after parthenogenetic activation , any abnormal chromosomes within fertilized oocytes were considered to be of sperm origin. Among the chromosome aberrations, we differentiated between minor (1 to 9 aberrations per karyoplates examined) and multiple (>9, scored always as 10 aberrations per oocyte). In addition to scoring normal versus abnormal karyoplates, we also calculated the incidence of chromosome aberrations, that is, aberration rate, which represents the total number of aberrations divided by the number of oocytes examined.
Sperm DNA fragmentation was assessed using a Trevigen Comet Assay kit (Trevigen, Gaithersburg, MD, USA, catalog no. 4250-050-K) under neutral conditions as previously described . One-hundred DNA tails were photographed and analyzed per slide and two males were analyzed per genotype. The length of each tail was measured from the center of the comet head to the end of the tail by Image J software  and classified into one of the four categories .
Transmission electron microscope analysis
Epididymal sperm were fixed in 2.5% glutaraldehyde, 0.1 M sodium cacodylate, 2 mM calcium chloride, pH 7.4, 1 h, then postfixed with osmium tetroxide (1% in 0.1 M cacodylate buffer, 1 h), dehydrated in ethanol, substituted with propylene oxide, and embedded in LX-112 epoxy resin. Ultra-thin sections (60 to 80 nm) were collected on Formvar-coated copper grids, double stained with uranyl acetate and lead citrate, and viewed with a LEO 912 (Zeiss) TEM, and photographed at 8,000× original magnification.
Preparation and analysis of sperm nuclear proteins by immunoblot
All extraction and preparation procedures were performed as described previously  except that sperm tails were removed by chemical treatment rather than sucrose centrifugation . The proteins were separated by electrophoresis in acid-urea 15% or 20% polyacrylamide gels and either stained with Coomassie blue or used for immunoblotting; an aliquot of sperm proteins corresponding to 4.5 × 106 cells was loaded per each lane. Antibody detection was performed as described previously . Briefly, the nuclear proteins were transferred to a nitrocellulose membrane in 7% acetic acid using Criterion wet blotting unit (BIORAD, Los Angeles, CA, USA). After blocking, the membrane was incubated for 2 h at room temperature with preP2 antibody recognizing the precursor domain of protamine 2  (1:9,000; courtesy of Marvin Meistrich, University of Texas) and/or antibody Hup2B detecting both protamine 2  (1:500,000; courtesy of Rod Balhorn, Lawrence Livermore Laboratories). Incubation with the corresponding secondary antibody conjugated with horseradish peroxidase and detection by chemiluminescence were carried out as described by the manufacturer (Amersham Pharmacia, Piscataway, NJ, USA). Band intensities (from Coomassie blue staining or western blot detection) were quantified using Photoshop software.
In the analysis of oocyte activation, oocyte arrest, and incidence of abnormal karyoplates, Mantel-Haenszel chi square test was used for 'within genotype' comparisons and Fisher's exact test was used to compare NPYq-deficient genotypes with their respective controls, and also to analyze the incidence of comet tail types and the TEM data. ANOVA (Generalized Linear Model as provided by NCSS Statistical Analysis Software (Kaysville, UT, USA)) with genotype, sperm source (epididymis or testis) and sperm status (fresh or frozen) as factors was used for the analysis of the oocyte activation data (after transforming percentage data to angles), comet tail lengths and for chromosome aberration rates, and for the analysis of western blot band intensities with gel and genotype as factors.
non-homologous end joining
mice with a deletion removing approximately two-thirds of NPYq
mice with a deletion removing approximately nine-tenths of NPYq
intracytoplasmic sperm injection
non-PAR: Y chromosome long arm, male specific Y chromosome long arm
mice lacking the entire NPYq.
This material is based on work supported by HCF Geist Foundation 20071382, NIH HD058059 and NIH 1 P20 RR024206-01 (Project 2) grants to MAW. We thank Angela Klaus from the Seton Hall University, NJ, and Tina Carvallo from the PBRC Biological Electron Microscope Facility at the University of Hawaii for help with interpretation of TEM results. We also thank Doug Carrell and Ben Emery from the University of Utah School of Medicine for sharing the protocol for sperm nuclear protein isolation. We are grateful to Rod Balhorn from the Lawrence Livermore Laboratories and Marvin Meistrich from the University of Texas for providing Hup2B and PreP2 antibodies, respectively. We thank Hiroyuki Tateno from Asahikawa Medical College, Japan, for providing Japanese brand pronase for oocyte preparation for chromosome analysis. We thank John Grove from the Department of Public Health at the University of Hawaii for help with the statistical analyses and we also thank students Kate Jaremko, Ashley Davidson, Samantha Wong and Sarah Mackenzie for participation in mice genotyping. Finally, we thank Julie Cocquet from MRC NIMR London, UK, for discussion on the manuscript.
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