Chromatin Spread Preparations for the Analysis of Mouse Oocyte Progression from Prophase to Metaphase II

Summary

Oogenesis in mammals is known to be error-prone, particularly due to chromosome missegregation. This manuscript describes chromatin spread preparation methods for mouse prophase, metaphase I and II-staged oocytes. These fundamental techniques allow for the study of chromatin-bound proteins and chromosome morphology throughout mammalian oogenesis.

Abstract

Chromatin spread techniques have been widely used to assess the dynamic localization of various proteins during gametogenesis, particularly for spermatogenesis. These techniques allow for visualization of protein and DNA localization patterns during meiotic events such as homologous chromosome pairing, synapsis and DNA repair. While a few protocols have been described in the literature, general chromatin spread techniques using mammalian prophase oocytes are limited and difficult due to the timing of meiosis initiation in fetal ovaries. In comparison, prophase spermatocytes can be collected from juvenile male mice with higher yields without the need for microdissection. However, it is difficult to obtain a pure synchronized population of cells at specific stages due to the heterogeneity of meiotic and post-meiotic germ cell populations in the juvenile and adult testis. For later stages of meiosis, it is advantageous to assess oocytes undergoing meiosis I (MI) or meiosis II (MII), because groups of mature oocytes can be collected from adult female mice and stimulated to resume meiosis in culture. Here, methods for meiotic chromatin spread preparations using oocytes dissected from fetal, neonatal and adult ovaries are described with accompanying video demonstrations. Chromosome missegregation events in mammalian oocytes are frequent, particularly during MI. These techniques can be used to assess and characterize the effects of different mutations or environmental exposures during various stages of oogenesis. As there are distinct differences between oogenesis and spermatogenesis, the techniques described within are invaluable to increase our understanding of mammalian oogenesis and the sexually dimorphic features of chromosome and protein dynamics during meiosis.

Introduction

During spermatogenesis, large semi-synchronous waves of meiotic germ cells are rapidly and continuously replenished in the testis at the onset of puberty and throughout adulthood¹. In contrast to males, meiosis in females is initiated solely during fetal development. Following birth, oocytes remain arrested in a prolonged dictyate stage of prophase I with an intact germinal vesicle (GV; nuclear envelope) until puberty. At the onset of puberty, a subset of oocytes are cyclically selected to undergo growth and maturation, marking the initiation of meiotic resumption. Meiotic resumption in fully-grown oocytes is manifested by the disappearance of the GV in a process known as germinal vesicle breakdown (GVBD). The oocyte then undergoes chromosome condensation and segregation, followed by polar body extrusion. Oocytes become arrested upon progression to MII and are stimulated to complete the second and final meiotic division only after fertilization.

Female fertility is highly dependent on the success of meiotic prophase I progression. Key to this is formation of a physical linkage between homologous chromosomes known as the chiasmata, which is mediated by repair of induced DNA double strand breaks (DSBs) via crossover recombination². This process occurs within the context of a dynamic protein-rich scaffold known as the synaptonemal complex (SC) that forms between homologous chromosomes to facilitate their synapsis³. The SC is a zipper-like tripartite structure that consists of two parallel lateral elements connected by central region proteins that holds homologs together throughout ongoing DNA repair. Prior to synapsis, precursors of the lateral elements, called axial elements, form between sister chromatids. Synaptonemal complex proteins such as SYCP2 and SYCP3 form axial elements that colocalize to the sister-chromatid cohesion axes during early prophase. These later serve as binding sites for the transverse filament protein, SYCP1, which facilitates central element assembly and synapsis between aligned homologs⁴. In mouse oocytes, complete synapsis is indicated by the presence of 20 completely overlapping SYCP3 and SYCP1 stretches, which can be visualized by using chromatin spread preparations. Synapsis is completed upon entry into the pachytene substage, whereby mature crossovers that are destined to form chiasmata between homologs are decorated with mutL homolog (MLH1/3) dimers to promote their accurate processing^5,6,7. The structural maintenance of chromosomes (SMC) complexes, including cohesin, condensin, and the SMC5/6 complex, are important for the regulation of chromosome dynamics and structure throughout meiosis^8,9,10,11,12. Collectively, these events ensure proper bi-orientation of homologous chromosomes to opposing spindle poles following disassembly of the SC.

The meiotic cell cycle is a powerful model to examine the roles of various proteins in genome maintenance due to the programmed induction and subsequent repair of DNA DSBs. Furthermore, mammalian meiosis is also a relevant model for the study of epigenetic modifications and imprinting¹³. However, it is technically difficult to assess these events during female meiosis, which takes place in fetal and neonatal ovaries in mammals (Figure 1). Prophase I can be divided into 5 substages: leptonema, zygonema, pachynema, diplonema and dictyate. Herein, we describe how to isolate and distinguish between fetal and neonatal ovaries and testes (Figure 2). Adapted from previously described methods, this manuscript also outlines a protocol (step 1) with video demonstration for preparation of female meiotic prophase I chromatin spreads^14,15,16,17. When coupled with immunolabelling, as described in steps 6-7, this protocol enables detailed microscopic analysis of prophase I events in oocytes.

Oogenesis is error-prone, and chromosome missegregation events during the first meiotic division represent the most common source of genetic disease in progeny^18,19. In this manuscript (protocol step 2), we describe a protocol in which mature GV-staged oocytes are extracted from primed ovaries of adult female mice. Under supportive conditions, fully-grown oocytes undergo luteinizing hormone-independent resumption of meiosis following isolation and culture²⁰. Following meiotic resumption, oocytes progress through meiosis I, then arrest at metaphase II. Oocytes remain arrested at metaphase II, unless fertilized. In steps 2–5, we adapt previously reported protocols with video demonstration to describe how to collect, culture and prepare MI and MII oocytes for chromatin spread preparations²¹. This chromatin spreading technique allows for clear immunolabelling of proteins associated with chromosomes. Furthermore, this protocol can also be used to distinguish between bivalent and univalent chromosomes, and can further resolve single sister chromatids to facilitate assessment of oocyte ploidy. Therefore, in addition to revealing localization patterns of meiotic proteins, this protocol can also serve as an invaluable tool for elucidating potential causes of chromosome missegregation during MI and MII.

Protocol

All methods described here have been approved by the Institutional Animal Care and Use Committee (IACUC) of Johns Hopkins University. Experiments were performed on wild-type C57BL/6J mice.

1. Harvesting Fetal or Neonatal Ovaries and Preparation of Prophase Chromatin Spreads

1. To extract embryos at 14.5–19.5 days post-coitum (dpc) sacrifice the pregnant females via cervical dislocation or CO₂ asphyxiation according to IACUC guidelines.
   NOTE: For postnatal day 1–5 ovaries skip to step 1.3. Figure 1 summarizes the meiotic prophase stages enriched at different embryonic and post-natal ages.
2. Open the abdominopelvic cavity using sterile scissors, making a V-shaped opening. Dissect out the maternal uterine horn, separate the embryos from the placenta, and transfer embryos into 35 mm petri dishes containing 3 mL of pre-warmed 1x phosphate buffer saline (PBS) at 37 °C.
   NOTE: A fliptop incubator set at 37 °C can be used to maintain temperature. In addition, a temperature regulated glass stage can also be used to maintain temperature during ovary manipulation.
3. With 3.5 inch surgical scissors, sacrifice embryos or pups via decapitation according to IACUC guidelines. Place decapitated embryos or pups in pre-warmed PBS prior to further dissection.
4. Dissect one embryo or pup at a time in a separate 35 mm petri dish containing 3 mL of pre-warmed PBS at 37 °C. Proceed by cutting along the ventral midline of the posterior half of the embryo, along the anterior half below the forelimbs and directly above the hind-limbs and tail as outlined in Figure 2A–B.
5. Open the abdomen using 3.5 inch surgical scissors. Using fine-tipped forceps displace or remove the liver and loops of bowel, exposing the ovaries in a new 35 mm petri dish containing 3 mL of pre-warmed PBS at 37 °C (see guide in Figure 2B). The ovaries are located immediately below and behind the kidney towards the posterior wall of the peritoneal cavity (Figure 2B–C). A guide for differentiating between male and female gonads is provided in Figure 2D.
   NOTE: For optimal conditions, rapidly dissect out the ovaries after pregnant female is sacrificed.
6. Remove both ovaries from each female fetus using a pair of fine-tipped forceps under a dissection scope and place in a watch glasses or separate wells of a multi-well plate containing 0.5 to 1.0 mL of pre-warmed PBS and maintain at 37 °C.
7. Place each pair of ovaries in 0.5 mL hypo-extraction buffer (17 mM trisodium citrate dihydrate, 50 mM sucrose, 5 mM EDTA, 0.5 mM DTT, 30 mM Tris-HCl, protease inhibitor, pH 8.2) in a clean watch glass or a small well of a 9-well plate, making sure to immerse the ovaries completely. Incubate for at least 15 min, but no more than 30 min.
   NOTE: Make hypo-extraction buffer fresh and use within 2 h of DTT addition.
8. During incubation, using a hydrophobic barrier PAP pen, draw two 22 x 22 mm² squares on a clean glass 25 x 75 mm², 1 mm thick microscope slide as shown in Figure 3A.
   NOTE: Slides can be prepared ahead of time.
9. Pipette 45–50 µL of 100 mM sucrose onto a clean slide and transfer one pair of ovaries to the drop.
10. Using the sharp ends of two 27 G needles, tease the ovaries apart to release cells into the sucrose solution. With forceps, remove large pieces of ovary and carefully pipette sucrose solution to disperse cells.
11. Place 40 µL of fixative solution (1% paraformaldehyde (PFA), 0.2% detergent (see Table of Materials), pH 9.2) into each square of the prepared slide. With a 200 µl pipette tip, spread the fixative solution evenly over the slide surface.
12. Pipette 20 µL of the sucrose mix onto the each square of the slide containing the fixative.
    NOTE: This equates to using one pair of ovaries per slide.
13. Incubate the slides in a closed humid chamber overnight at room temperature.
    NOTE: The overnight incubation can range around (12-15 hrs) at room temperature.
14. Open the chamber lid and allow the slides to air-dry completely.
15. Wash slides in a Coplin jar containing 50 mL of 0.4% wetting agent-PBS solution (see Table of Materials) for 2 min, air dry, and proceed to immunolabelling protocol (step 6).
    NOTE: It may be possible to store the slides at -80 °C for later use, but this varies depending on the protein of interest. For optimal results proceed immediately to the immunolabelling protocol (step 6).

2. Metaphase I Oocyte Collection

1. To maximize the number of antral follicles isolated from each mouse, intraperitoneally inject sexually mature virgin female mice with 5 IU of pregnant mare's serum gonadotropin (PMSG, also known as equine chorionic gonadotropin (eCG)).
   NOTE: For optimal oocyte yield, mice should be 1 to 3 months of age, as the number of oocytes harvested will decrease with age. To prepare PMSG, dissolve bottle of 5,000 IU in 100 mL of sterile PBS (5 U/0.1 mL) Store in single-use aliquots of 600 µL at -20 °C.
2. After 44–48 h, prepare collection medium, minimum essential medium alpha (MEMα) medium supplemented with 5% fetal bovine serum (FBS) and 3 mg/mL bovine serum albumin (BSA; MEMα/BSA/FBS). Sterilize media through a 0.2 µm pore filter. Decant 2.5 mL of MEMα/BSA/FBS medium into one glass dish per mouse and warm to 37 °C in a 5% CO₂ incubator.
   NOTE: Other collection and culture media that are commercially available (M2 and M16) are also commonly used.
   Caution: We recommend removing culture dishes from the 5% CO₂ incubator one at a time for limited duration to minimize ambient air exposure during manipulation steps.
3. Sacrifice the mice via cervical dislocation or CO₂ asphyxiation according to IACUC guidelines.
4. Open the abdominopelvic cavity using sterile scissors, making a large V-shaped opening. Using forceps, displace intestines towards the head of the mouse. Locate each uterine horn; the ovaries are present proximal to the rib cage. Hold the oviduct with fine forceps and cut the fat superior to the ovary using dissection scissors (Figure 4). Continue to hold the oviduct, and with another set of fine forceps release the ovary from the bursa and place into collection dish containing MEMα/BSA/FBS medium.
   NOTE: As in step 1, it is imperative to keep the ovaries at 37 °C and maintain at 5% CO₂. A fliptop incubator hooked up to 5% CO₂ mix can be used to allow for optimal maintenance of temperature and CO₂ levels. In addition, a temperature regulated glass stage should also be used to maintain temperature during oocyte manipulation.
5. Using a 1 mL syringe with a 27-gauge needle (or similar size), release cumulus oocyte complexes by manually puncturing the large antral follicles.
6. While observing through a dissection microscope, collect GV-staged oocytes using a mouth-operated glass pipette or capillary, or a hand-operated micrometer-syringe (Figure 5). Only collect oocytes that are released from antral follicles. GV oocytes have a diameter of approximately 90 µm. GV oocytes may be surrounded by 2-3 layers of granulosa cells, and have a total diameter of around 200 µm.
7. Culture oocytes in a clean watch glass or a 9-well plate containing MEMα/BSA/FBS medium for 6 h to reach metaphase I at 37 °C in a 5% CO₂ incubator.
8. Proceed to step 4.

3. Metaphase II (MII) Oocyte Collection

1. To maximize oocytes isolated from each mouse, intraperitoneally inject sexually mature virgin female mice with 5 IU of PMSG. After 44–48 h, intraperitoneally inject with 5 IU of human chorionic gonadotropin (hCG).
   NOTE: For optimal oocyte yield, mice should be 1 to 3 months of age, as the number of oocytes harvested will decrease with age. To prepare hCG, dissolve a bottle of 10,000 U in 200 mL PBS (5 U/0.1 mL). Store in single-use aliquots of 600 µL at -20 °C.
2. After 12-14 hrs, prepare MEMα/BSA/FBS collection medium, as described in step 2.2, above.
3. Sacrifice the mice via cervical dislocation or CO₂ asphyxiation according to IACUC guidelines.
4. Open the abdominopelvic cavity using sterile scissors, making a large V-shaped opening. Using forceps, displace intestines towards the head of the mouse. Locate each uterine horn, the ovaries are present proximal to the rib cage. Hold the oviduct with fine forceps and cut the fat superior to the ovary using dissection scissors (Figure 4). Then remove the ovary and oviduct and place into collection dish containing MEMα/BSA/FBS medium.
   NOTE: As in steps 1 and 2, it is imperative to keep the ovaries at 37 °C and maintain at 5% CO₂. A fliptop incubator hooked up to 5% CO₂ mix can be used to allow for optimal maintenance of temperature and CO₂ levels. In addition, a temperature regulated glass stage should also be used to maintain temperature during oocyte manipulation.
5. Using a 1 mL syringe with a 27 G (or similar size) or sharp forceps, tear a hole in the ampulla of the oviduct to release the MII oocytes.
   NOTE: Be careful not to damage the oocytes in the ampulla. The ampulla will appear swollen and translucent such that the oocytes are visible (Figure 4).
6. Harvest MII oocytes from the ampulla of the oviduct into a new dish with collection medium using a mouth-operated glass pipette or capillary, or a hand-operated micrometer-syringe (Figure 5).
7. Proceed to step 4.

4. Oocyte Denuding and Zona Pellucida Removal

1. Prepare 300 IU/mL of hyaluronidase in MEMα medium supplemented with 3 mg/mL BSA to denude oocytes of surrounding cumulus cells (2.5 mL/mouse) in a watch glass, and keep at 37 °C, 5% CO₂.
   NOTE: Hyaluronidase efficacy sharply decreases after 1 h of preparation. For MII oocytes, hyaluronidase treatment is not required.
2. Expose oocyte-cumulus cell complexes to 300 IU/mL of hyaluronidase in MEMα/BSA for 3 min to denude oocytes of surrounding cumulus cells.
   Caution: Do not exceed 3 min exposure to hyaluronidase, as it will damage the oocytes.
3. To wash the oocytes, transfer oocytes to a fresh warmed MEMα/BSA medium dish. Using a small mouth-operated glass pipette or capillary (slightly larger than the diameter of the oocyte, which is approximately 90 µm), pipette the complexes up and down to completely detach the cumulus cells. Allow the oocytes to recover in the incubator while preparing for the next step.
4. Warm acidic Tyrode's solution, MEMα/BSA, and Waymouth's media to 37 °C (500 µL/mouse). Place 300 µL in each well of small 9-well glass plates.
5. To remove the zona pellucida (ZP) transfer 5–10 oocytes into Tyrode's solution. Expose the oocytes for only 30-45 s to the solution.
   NOTE: Too little exposure to the solution will not remove the ZP completely, which will prevent the oocytes from bursting and chromosomes from spreading. Too much exposure will damage and kill the oocyte. Watching the ZP dissolve under the dissection microscope can aid in optimizing exposure time.
   Caution: Using fresh Tyrode's solution is critical, as its function declines with age. Use a fresh well of Tyrode's solution for each group of oocytes treated to ensure uniform digestion of the ZP.
6. Immediately after ZP removal, wash the oocytes by transferring into warmed MEMα/BSA/FBS medium. Repeat this wash step.
   NOTE: Be careful when transferring, as oocytes will easily stick together and to the glass pipette or capillary following removal of the ZP. Pre-wetting the glass pipette or capillary in Waymouth's medium will minimize oocytes sticking together.
7. Transfer and allow the oocytes to recover for 30 minutes in Waymouth's medium at 37 °C in a 5% CO₂ incubator.
8. Proceed to step 5.

5. MI and MII Oocyte Chromatin Spreads

1. Using a PAP pen, draw a 11 x 44 mm² rectangle on the glass slide as shown in Figure 6A.
2. Coat the slide with a thin layer of fixative (1% paraformaldehyde, 0.2% Triton-X 100 in H₂O, pH 9.2) by pipetting 100 µL of fixative onto the slide and rocking the slide back and forth. Tap the slide to get rid of excess fixative.
3. Pick up between 5-10 oocytes with a small mouth pipette needle with as little media as possible and drag the needle in a line across the fixative-coated slide while depositing the oocytes from 1 cm above the slide into the fixative solution. Perform this step using a dissection microscope to ensure that the oocytes have been deposited and that they have burst.
   NOTE: The oocytes should burst immediately on the slide. The height at which the oocytes are deposited impact the degree of chromatin spreading. See representative results in Figure 6 for further details.
4. Incubate slides at room temperature in a closed humidified chamber overnight to allow the chromatin to adhere.
5. Allow the slides to air-dry completely and rinse slides in a Coplin jar containing 50 mL of 0.4% wetting agent-H₂O, pH 8.0.
6. Proceed to step 6.

6. Immunolabelling

1. Prepare the antibody dilution buffer (ADB) described in Table 1.
2. Prepare two Coplin jars containing 50 mL of wash buffer (WB) solution (10% ADB diluted in PBS), and one Coplin jar containing 50 mL WB and 0.05% detergent solution (e.g., add 250 µL of 10% detergent to 50 mL WB).
3. Wash the slides that were prepared in section 1 and 5 of this protocol for 10 min in one Coplin jar containing 50 mL of WB.
   Caution: Do not let the slides dry at any point during immunolabelling.
4. Wash the slides for 10 min in the Coplin jar containing 50 mL WB and 0.05% detergent solution. Then, wash the slides in the remaining Coplin jar containing 50 mL of WB solution for 10 min.
5. Tap off excess liquid and cover slide with 100 µL of selected primary antibodies diluted in ADB. Incubate at 4 °C overnight in a closed humid chamber.
   NOTE: Incubation can be shortened to 2 to 3 hrs at 37 °C. Use smaller volumes of antibody (e.g., 50 µL) by covering the slide with a coverslip or parafilm.
6. Rinse slides in a Coplin jar containing 50 mL of 0.2% wetting agent-PBS solution, pH 8.0.
7. Repeat steps 6.2 to 6.5.
8. Tap off excess liquid and cover slide with 100 µL of selected secondary antibodies diluted in ADB. Incubate slides 1 to 2 hrs at 37 °C in a closed humid chamber.
9. Wash slides 2 times for 10 min in Coplin jars containing 50 mL of 0.2% wetting agent-PBS solution, pH 8.0.
10. Wash slides 2 times for 5 min in Coplin jars containing 50 mL of 0.2% wetting agent-H₂O solution, pH 8.0.

7. Mounting slides

1. For prophase chromatin spreads prepared in step 2, add 100 µL of mounting medium containing 4', 6-diamidino-2-phenylindole (DAPI, 1.5µg/mL). For MI and MII chromatin spreads prepared in step 5, add 50 µL of mounting medium containing DAPI (1.5µg/mL). Gently blot away excess liquid.
2. Place a 22 mm x 60 mm coverslip on top and seal with clear nail polish. Store in a slide box at 4 °C or -20 °C until assessment via fluorescence microscopy.
   NOTE: Tap lightly on cover slip to rid of excess mounting medium before sealing with nail polish.

Results

We have described two techniques for visualizing and assessing meiotic chromosomes in oocytes. The first technique is catered toward assessing prophase progression in embryonic and neonatal ovaries. Prophase chromatin spread preparations are incredibly valuable for visualizing numerous dynamic processes during meiosis, including chromosome pairing, synapsis and desynapsis, homologous recombination, and epigenetic chromosome remodeling. Here, we have demonstrated the utility of this method...

Discussion

Chromatin spread preparations allow researchers to chronologically study female mammalian meiosis and the dynamic localization of proteins involved. The embryonic and neonatal chromatin spreads allow for close analysis of events throughout meiotic prophase. Metaphase I and metaphase II chromatin spreads can be used to distinguish single sister chromatids from paired sisters and paired homologous chromosomes, as well as assess ploidy. By comparison, the protocol described here can be advantageous compared to whole oocyte ...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
10X Phosphate buffered saline (PBS) pH 7.4	Quality Biological	119-069-161
60 mm x 15 mm petri dishes	Denville	T1106
35mm x 12mm petri dishes	Denville	T1103
Fine forceps	VWR	300-050
Micro dissection scissors	Ted Pella	1340
Dissecting scissors, sharp tip, 41/2"	VWR	82027-578
Watch glass square 1 5/8	Carolina Biological Supply Company	742300	Autoclave before each use
Sucrose	Sigma	S8501
Trisodium Citrate Dihydrate	Sigma	S1804
EDTA	Sigma	E6758
Trizma Base	Sigma	T1503
1,4-Dithiothreitol (DTT)	Sigma	646563	Add to hypotonic buffer immediately before use
50x Protease Inhibitor	Roche	11873580001	Add to hypotonic buffer immediately before use
Turberculin syringe with needle (1cc, 27 G x 1/2 in)	Becton, Dickinson (BD)	309623
Gold seal ultra frost glass slides (25X75mm, 1mm thick)	Thermo	3063-002
Super PAP pen, large (liquid blocker)	Electron Microscopy Sciences (EMS)	71310
16% Paraformaldehyde aqueous	Electron Microscopy Sciences (EMS)	15710
Triton X-100	Sigma	T8787	Detergent in manuscript
Immuno stain moisture chamber	Evergreen	240-9020-Z10
Coplin jars	Fisher	08-815
Photo-flo 200	Electron Microscopy Sciences (EMS)	74257	Wetting agent in manuscript
Pregnant mare serum gonadotropin (PMSG)	Sigma	G4877	Store aliquots at -20C
Human chorionic gonadotropin (HCG)	Sigma	C0434	Store aliquots at -20C
PYREX Spot Plates with nine concave cavities	Fisher	13-748B	Autoclave before each use
Glass capillary	Fisher	22260943	For making oocyte collection needles
Brand Parafilm M	Sigma	BR701501	For making oocyte collection needles
Latex rubber tubing (3.2 mm inner diameter x 6.4 mm outer diameter)	Fisher	14-178-5B	For making oocyte collection needles
Latex rubber tubing (6.4 mm inner diameter x 11.1 mm outer diameter)	Fisher	14-178-5D	For making oocyte collection needles
Flexible silicone rubber nosepiece, hard plastic mouthpiece and 15 inches of latex tubing	Sigma	A5177-5EA	For making oocyte collection needles
Mitutoyo micrometer head	Mituoyo	150-208	For making oocyte collection needles
Syringe 5 mL	BD Biosciences	309646	For making oocyte collection needles
Syringe filter 0.45 μm filter	Corning	431220	For making oocyte collection needles
Glass Pasteur Pipette 5 3/4"	Fisher	13-678-6A	For making oocyte collection needles
83 x 0.5 mm pipette tip	Denville	P3080	For making oocyte collection needles
α-MEM	Invitrogen	11415049
Waymouth's media	Life Technologies	11220035
Fetal bovine serum	Fisher	A3160602
Bovine serum albumin (BSA)	Sigma	A3311	For oocyte culture media
500ml filter units 0.22um	Denville	F5227
Hyaluronidase	Sigma	H3506
Tyrode’s solution	Sigma	T1788	Store aliquots at -20C
Horse serum	Sigma	H-1270	For ADB/wash buffer
Bovine serum albumin (BSA)	Sigma	A1470	For ADB/wash buffer
VECTASHIELD antifade mounting medium with DAPI	Vector Labs	H-1200
Microscope cover slides (22mmx60mm)	Fisher	12-544-G
Clear nail polish	Amazon	N/A
Name	Company	Catalog Number	Comments
Microscopes
SteREO Discovery.V8	Zeiss	495015-0001-000
Observer Z1	Zeiss
Name	Company	Catalog Number	Comments
Primary Antibodies
Mouse anti-MLH1	Life Technologies	MA5-15431	Dilution factor- 1:100
Rabbit anti-SYCP1	Life Technologies	PA1-16763	Dilution factor- 1:1000
Goat anti-SCP3	Santa Cruz	sc-20845	Dilution factor- 1:50
Human anti-centromere protein	Antibodies Incorporated	15-235	Dilution factor- 1:100
Rabbit anti- TOPOII	Abcam	ab109524	Dilution factor- 1:100
Mouse anti-Histone H4 (di methyl K20, tri methyl K20)	Abcam	ab78517	Dilution factor- 1:500
Rabbit anti-Rec8	Courtesy of Dr. Karen Schindler	N/A	Dilution factor- 1:10,000
Name	Company	Catalog Number	Comments
Secondary Antibodies
Donkey anti-goat IgG (H+L) Alexa Fluor 568 conjugate	Thermo-Fisher Scientific	A-11057	Dilution factor- 1:500
Donkey anti-mouse IgG (H+L) Alexa Fluor 488 conjugate	Thermo-Fisher Scientific	A-21202	Dilution factor- 1:500
Donkey anti-rabbit IgG (H+L) Alexa Fluor 647 conjugate	Thermo-Fisher Scientific	A-31573	Dilution factor- 1:500
Goat anti-mouse IgG (H+L) Alexa Fluor 568 conjugate	Thermo-Fisher Scientific	A-11004	Dilution factor- 1:500
Goat anti-Human IgG (H+L) Cross-Adsorbed Secondary Antibody, Alexa Fluor 488	Thermo-Fisher Scientific	A-11013	Dilution factor- 1:500
Goat anti-rabbit IgG (H+L) Alexa Fluor 568 conjugate	Thermo-Fisher Scientific	A-11011	Dilution factor- 1:500