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Nuclear surface spreads are an indispensable tool for studying chromosome events during meiosis. Here we demonstrate a method to prepare and visualize meiotic chromosomes during prophase I from zebrafish spermatocytes.
Meiosis is the key cellular process required to create haploid gametes for sexual reproduction. Model organisms have been instrumental in understanding the chromosome events that take place during meiotic prophase, including the pairing, synapsis, and recombination events that ensure proper chromosome segregation. While the mouse has been an important model for understanding the molecular mechanisms underlying these processes, not all meiotic events in this system are analogous to human meiosis. We recently demonstrated the exciting potential of the zebrafish as a model of human spermatogenesis. Here we describe, in detail, our methods to visualize meiotic chromosomes and associated proteins in chromosome spread preparations. These preparations have the advantage of allowing high resolution analysis of chromosome structures. First, we describe the procedure for dissecting testes from adult zebrafish, followed by cell dissociation, lysis, and spreading of the chromosomes. Next, we describe the procedure for detecting the localization of meiotic chromosome proteins, by immunofluorescence detection, and nucleic acid sequences, by fluorescence in situ hybridization (FISH). These techniques comprise a useful set of tools for the cytological analysis of meiotic chromatin architecture in the zebrafish system. Researchers in the zebrafish community should be able to quickly master these techniques and incorporate them into their standard analyses of reproductive function.
Sexual reproduction proceeds through the combination of two haploid gametes, each carrying half the chromosome complement of a somatic cell. Meiosis is a specialized cell division that produces haploid gametes through one round of DNA replication and two successive rounds of chromosome segregation. In prophase I, homologous chromosomes (homologs) must undergo pairing, recombination, and synapsis, the latter of which is characterized by the formation of the synaptonemal complex that comprises two homolog axes bridged by the transverse filament, Sycp1 (Figure 1A,B). Failure to properly execute these processes can lead to the production of aneuploid game....
All methods involving zebrafish were carried out using ethical standards approved by the Institutional Animal Care and Use Committee at UC Davis.
1. Chromosome spreading procedure
NOTE: The following protocol is designed to create 4-6 slides, with hundreds of spread meiotic nuclei per slide. The numbers of testes used will depend on the size of the fish. Expect to use 20 animals at ~60 days post fertilization (dpf) and 15 animals at ~6 months post fertilization (mpf)........
We have outlined a method to prepare and visualize zebrafish spermatocyte spread preparations. When performed correctly, our procedure yields well spread, non-overlapping nuclei. To recover such nuclei, it is important to have the appropriate amount of starting material (i.e., testes), treat testes for a sufficient length of time in trypsin and an adequate number of DNase I treatments. These spreads can then be stained for telomeres and meiotic proteins to study meiotic progression during.......
Here we describe methods to probe the location of telomeres and chromosome-associated proteins in nuclear surface spreads from spermatocytes isolated from zebrafish testes. We expect that these methods will be applicable for analysis of spermatocytes in other teleost species with adjustment to the size of the testis.
While only a few antibodies have been raised to zebrafish meiotic proteins, we have had success using the following antibodies raised to human (h) or mouse (m) proteins. Our lab h.......
We thank Trent Newman and Masuda Sharifi for comments on the manuscript and An Nguyen for helping to optimize methods for spreading and staining chromosomes from zebrafish meiocytes. This work was supported by NIH R01 GM079115 awarded to S.M.B.
....Name | Company | Catalog Number | Comments |
1.5 mL centrifuge tubes | Several commercial brands available | ||
1.5 mL microcentrifuge tube rack | Several commercial brands available | ||
16% formaldehyde, methanol-free | ThermoFisher Scientific | 28908 | |
2 mL | Several commercial brands available | ||
24 x 50 mm glass coverslips | Corning | 2980-245 | |
24 x 60 mm glasscoverslips | VWR International | 16004-312 | |
50 mL conical centrifuge tubes | ThermoFisher Scientific | 363696 | |
Autoclave bag | Several commercial brands available | Used to make plastic coverslips. | |
Bovine Serum Albumin (BSA) | Fisher Scientific | BP1605-100 | Prepare a 100 mg/ml stock solution in sterile distilled water. |
Cell Strainer, 100 µm | Fisher Scientific | 08-771-19 | |
CF405M goat anti-chicken IgY (H+L), highly cross-adsorbed | Biotium | 203775-500uL | Use at 1:1000 |
Chicken anti-zfSycp1 | Generated by Burgess lab | N/A | Use at 1:100 |
Collagenase from Clostridium histolyticum | Sigma-Aldrich | C0130-500MG | |
Coplin jar | Several commercial brands available | ||
DNase I, grade II from bovine pancreas | Roche Diagnostics | 10104159001 | |
Dulbecco's Modified Eagle Medium (DMEM) | Fisher Scientific | MT10014CV | |
Dumont No. 5 Forceps | Fine Science Tools | 11252-30 | Two are required for dissecting the testes. |
Eppendorf Tubes, 5 mL | VWR International | 89429-308 | |
Formamide | Fisher Scientific | BP228-100 | |
Goat anti-chicken IgY (H+L) secondary antibody, Alexa Fluor 488 | ThermoFisher Scientific | A-11039 | Use at 1:1000 |
Goat anti-chicken IgY (H+L) secondary antibody, Alexa Fluor 594 | ThermoFisher Scientific | A-11042 | Use at 1:1000 |
Goat anti-hDMC1 | Santa Cruz Biotechnology | sc-8973 | Does not work in our hands |
Goat anti-rabbit IgG (H+L) cross-adsorbed secondary antibody, Alexa Fluor 488 | ThermoFisher Scientific | A-11008 | Use at 1:1000 |
Goat anti-rabbit IgG (H+L) cross-adsorbed secondary antibody, Alexa Fluor 594 | ThermoFisher Scientific | A-11012 | Use at 1:1000 |
Goat serum | Sigma-Aldrich | G9023-10mL | |
Heparin sodium salt | Sigma-Aldrich | H3393-100KU | |
Humidity chamber | Fisher Scientific | 50-112-3683 | |
Hybridization Oven | VWR International | 230401V (Model 5420) | |
Incubator Shaker | New Brunswick Scientific | Model Classic C25 | |
KCl | Fisher Scientific | P217-500 | |
Kimwipes | Kimerbly-Clark Professional | 34155 | Used for the humidity chamber |
KH2PO4 | Fisher Scientific | P285-500 | |
Microscope | Several commercial brands available | Any standard microscope capable of at least ~1.65X magnification is sufficient. | |
Microscope slides | Fisher Scientific | 12-544-7 | |
Mouse anti-hamsterSCP3 | Abcam | ab97672 | Does not work in our hands |
Mouse anti-hMLH1 | BD Biosciences | 550838 | Does not work in our hands |
Mouse anti-hRPA | Sigma-Alrich | MABE285 | Does not work in our hands |
Na2HPO4 · 7 H2O | Fisher Scientific | S373-500 | |
NaCl | Fisher Scientific | S271-3 | |
Photo-Flo 200 solution | Electron Microscopy Sciences | 74257 | |
Plastic transfer pipettes | Several commercial brands available | ||
PNA TelC-Alexa647 | PNA Bio Inc | F1013 | Prepare as per manufacturer's instructions. |
PNA TelC-Cy3 | PNA Bio Inc | F1002 | Prepare as per manufacturer's instructions. |
ProLong Diamond Antifade Mountant | ThermoFisher Scientific | P36970 | |
ProLong Diamond Antifade Mountant with DAPI | ThermoFisher Scientific | P36971 | |
Rabbit anti-hRPA | Bethyl | A300-244A | Use at 1:300 |
Rabbit anti-hSCP3 | Abcam | ab150292 | Use at 1:200 |
Rabbit anti-hRad51 | GeneTex | GTX100469 | Use at 1:300 |
Sodium citrate | Fisher Scientific | S279-500 | |
Sucrose | Fisher Scientific | S5-500 | |
Supercut Scissors, 30° angle, 10 cm | Fisher Scientific | 50-822-353 | Can also use any pair of small scissors. |
Sylgard kit | Fisher Scientific | NC9897184 | Prepare as per manufacturer's instructions. |
Triton X-100 | Fisher Scientific | BP151-100 | Dilute in sterile distilled water to make a 20% working solution. Store at room temperature. Triton X-100 forms a precipitate when diluted in water; precipitate dissolves overnight. |
Trypsin | Worthington Biochemical | LS003708 | |
Trypsin inhibitor from chicken egg white | Sigma-Aldrich | T9253-500MG | |
Tween 20 | Bio-Rad | 170-6531 | Dilute in sterile distilled water to make a 20% working solution. Store at room temperature. |
Vannas Spring Scissors - 4 mm (micro scissors) | Fine Science Tools | 15018-10 |
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