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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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....

Protocol

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)........

Representative Results

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.......

Discussion

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.......

Acknowledgements

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.

....

Materials

NameCompanyCatalog NumberComments
1.5 mL centrifuge tubesSeveral commercial brands available
1.5 mL microcentrifuge tube rackSeveral commercial brands available
16% formaldehyde, methanol-freeThermoFisher Scientific28908
2 mLSeveral commercial brands available
24 x 50 mm glass coverslipsCorning2980-245
24 x 60 mm glasscoverslipsVWR International16004-312
50 mL conical centrifuge tubesThermoFisher Scientific363696
Autoclave bagSeveral commercial brands availableUsed to make plastic coverslips.
Bovine Serum Albumin (BSA)Fisher ScientificBP1605-100Prepare a 100 mg/ml stock solution in sterile distilled water.
Cell Strainer, 100 µmFisher Scientific08-771-19
CF405M goat anti-chicken IgY (H+L), highly cross-adsorbedBiotium203775-500uLUse at 1:1000
Chicken anti-zfSycp1Generated by Burgess labN/AUse at 1:100
Collagenase from Clostridium histolyticumSigma-AldrichC0130-500MG
Coplin jarSeveral commercial brands available
DNase I, grade II from bovine pancreasRoche Diagnostics10104159001
Dulbecco's Modified Eagle Medium (DMEM)Fisher ScientificMT10014CV
Dumont No. 5 ForcepsFine Science Tools11252-30Two are required for dissecting the testes.
Eppendorf Tubes, 5 mLVWR International89429-308
FormamideFisher ScientificBP228-100
Goat anti-chicken IgY (H+L) secondary antibody, Alexa Fluor 488ThermoFisher ScientificA-11039Use at 1:1000
Goat anti-chicken IgY (H+L) secondary antibody, Alexa Fluor 594ThermoFisher ScientificA-11042Use at 1:1000
Goat anti-hDMC1Santa Cruz Biotechnologysc-8973Does not work in our hands
Goat anti-rabbit IgG (H+L) cross-adsorbed secondary antibody, Alexa Fluor 488ThermoFisher ScientificA-11008Use at 1:1000
Goat anti-rabbit IgG (H+L) cross-adsorbed secondary antibody, Alexa Fluor 594ThermoFisher ScientificA-11012Use at 1:1000
Goat serumSigma-AldrichG9023-10mL
Heparin sodium saltSigma-AldrichH3393-100KU
Humidity chamberFisher Scientific50-112-3683
Hybridization OvenVWR International230401V (Model 5420)
Incubator ShakerNew Brunswick ScientificModel Classic C25
KClFisher ScientificP217-500
KimwipesKimerbly-Clark Professional34155Used for the humidity chamber
KH2PO4Fisher ScientificP285-500
MicroscopeSeveral commercial brands availableAny standard microscope capable of at least ~1.65X magnification is sufficient.
Microscope slidesFisher Scientific12-544-7
Mouse anti-hamsterSCP3Abcamab97672Does not work in our hands
Mouse anti-hMLH1BD Biosciences550838Does not work in our hands
Mouse anti-hRPASigma-AlrichMABE285Does not work in our hands
Na2HPO4 · 7 H2OFisher ScientificS373-500
NaClFisher ScientificS271-3
Photo-Flo 200 solutionElectron Microscopy Sciences74257
Plastic transfer pipettesSeveral commercial brands available
PNA TelC-Alexa647PNA Bio IncF1013Prepare as per manufacturer's instructions.
PNA TelC-Cy3PNA Bio IncF1002Prepare as per manufacturer's instructions.
ProLong Diamond Antifade MountantThermoFisher ScientificP36970
ProLong Diamond Antifade Mountant with DAPIThermoFisher ScientificP36971
Rabbit anti-hRPABethylA300-244AUse at 1:300
Rabbit anti-hSCP3Abcamab150292Use at 1:200
Rabbit anti-hRad51GeneTexGTX100469Use at 1:300
Sodium citrateFisher ScientificS279-500
SucroseFisher ScientificS5-500
Supercut Scissors, 30° angle, 10 cmFisher Scientific50-822-353Can also use any pair of small scissors.
Sylgard kitFisher ScientificNC9897184Prepare as per manufacturer's instructions.
Triton X-100Fisher ScientificBP151-100Dilute 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.
TrypsinWorthington BiochemicalLS003708
Trypsin inhibitor from chicken egg whiteSigma-AldrichT9253-500MG
Tween 20Bio-Rad170-6531Dilute in sterile distilled water to make a 20% working solution. Store at room temperature.
Vannas Spring Scissors - 4 mm (micro scissors)Fine Science Tools15018-10

References

  1. Nagaoka, S. I., Hassold, T. J., Hunt, P. A. Human aneuploidy: mechanisms and new insights into an age-old problem. Nature Reviews Genetics. 13, 493-504 (2012).
  2. Zickler, D., Kleckner, N. Recombination, Pairing, and Synap....

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Meiotic Chromosome SpreadsZebrafish SpermatocytesVertebrate ModelMeiosisHomologous Chromosome PairingSynapsisRecombinationSuper Resolution MicroscopyDissectionTestesCollagenaseDMEMSucrose SolutionCell Dissociation

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