Lampbrush chromosomes of Danio rerio
Jazyk angličtina Země Nizozemsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
#MK-3553.2022.1.4
research grant
#MK-3553.2022.1.4
research grant
RVO 67985904
Akademie Věd České Republiky
PubMed
39815120
DOI
10.1007/s10577-024-09761-z
PII: 10.1007/s10577-024-09761-z
Knihovny.cz E-zdroje
- Klíčová slova
- Centromere, FISH-mapping, Germinal vesicle, Histone locus bodies, Karyotype analysis, Lampbrush chromosomes, Non-coding RNA, Oocyte nucleus, Tandem repeats, Telomere, Zebrafish,
- MeSH
- chromozomy * MeSH
- dánio pruhované * genetika MeSH
- hybridizace in situ fluorescenční MeSH
- karyotyp MeSH
- karyotypizace MeSH
- oocyty metabolismus MeSH
- ribonukleoproteiny genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- ribonukleoproteiny MeSH
Danio rerio, commonly known as zebrafish, is an established model organism for the developmental and cell biology studies. Although significant progress has been made in the analysis of the D. rerio genome, cytogenetic studies face challenges due to the unclear identification of chromosomes. Here, we present a novel approach to the study of the D. rerio karyotype, focusing on the analysis of lampbrush chromosomes isolated from growing oocytes. Lampbrush chromosomes, existing during diplotene, serve as a powerful tool for high-resolution mapping and transcription analysis due to their profound decondensation and remarkable lateral loops decorated by RNA polymerases and ribonucleoprotein (RNP) matrix. In D. rerio, lampbrush chromosomes are about 20 times longer than corresponding metaphase chromosomes. We found that the lampbrush chromosome stage karyotype of D. rerio is generally undifferentiated, except for several bivalents bearing distinct marker structures, including loops with complex RNP matrix and locus-associated nuclear bodies. Locus-associated nuclear bodies were enriched for coilin and snRNAs; the loci where they formed presumably correspond to the histone gene clusters. Further, we observed the accumulation of splicing factors in giant terminal RNP aggregates on one bivalent. DAPI staining of Danio rerio lampbrush chromosomes revealed large and small chromomeres non-uniformly distributed along the axis. For example, D. rerio lampbrush chromosome 4, comprising the sex-determining region, is divided into two halves-with small chromomeres bearing long lateral loops and with large dense chromomeres bearing no or very tiny lateral loops. As centromeres were not distinguishable, we identified centromeric regions in all bivalents by FISH mapping of pericentromeric RFAL1, RFAL2, and RFAM tandem repeats. Through a combination of morphological analysis, immunostaining of marker structures, and centromere mapping, we developed cytological maps of D. rerio lampbrush chromosomes. Finally, by RNA FISH we revealed transcripts of pericentromeric and telomeric tandem repeats at the lampbrush chromosome stage.
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Aharon D, Marlow FL (2021) Sexual determination in zebrafish. Cell Mol Life Sci 79:8 PubMed DOI PMC
Anderson JL, Marí AR, Braasch I, Amores A, Hohenlohe P, Batzel P, Postlethwait JH (2012) Multiple sex-associated regions and a putative sex chromosome in zebrafish revealed by RAD mapping and population genomics. PLoS ONE 7:e40701 PubMed DOI PMC
Avdesh A, Chen M, Martin-Iverson MT, Mondal A, Ong D, Rainey-Smith S, Taddei K, Lardelli M, Groth DM, Verdile G, Martins RN (2012) Regular care and maintenance of a zebrafish (Danio rerio) laboratory: an introduction. J Vis Exp:4196. https://doi.org/10.3791/4196
Azzalin CM, Lingner J (2015) Telomere functions grounding on TERRA firma. Trends Cell Biol 25:29–36 PubMed DOI
Barman RP (1991) A taxonomic revision of the Indo-Burmese species of Danio Hamilton Buchanan (pisces, Cyprinidae). Zoological Survey of India, University of California, 91
Baumeister HG (1973) Lampbrush chromosomes and RNA-synthesis during early oogenesis of Brachydanio rerio (cyprinidae, teleostei). Z Für Zellforsch Mikrosk Anat 145:145–150 DOI
Blokhina YP, Nguyen AD, Draper BW, Burgess SM (2019) The telomere bouquet is a hub where meiotic double-strand breaks, synapsis, and stable homolog juxtaposition are coordinated in the zebrafish, Danio rerio. PLOS Genet 15:e1007730 PubMed DOI PMC
Blokhina YP, Frees MA, Nguyen A, Sharifi M, Chu DB, Bispo K, Olaya I, Draper BW, Burgess SM (2021) Rad21l1 cohesin subunit is dispensable for spermatogenesis but not oogenesis in zebrafish. PLOS Genet 17:e1009127 PubMed DOI PMC
Bradley KM, Breyer JP, Melville DB, Broman KW, Knapik EW, Smith JR (2011) An SNP-based linkage map for zebrafish reveals sex determination loci. G3 Genes|Genomes|Genetics 1:3–9 DOI
Bucci S, Ragghianti M, Mancino G, Berger L, Hotz H, Uzzell T (1990) Lampbrush and mitotic chromosomes of the hemiclonally reproducing hybrid Rana esculenta and its parental species. J Exp Zool 255:37–56 PubMed DOI
Callan HG (1986) Lampbrush chromosomes. Mol Biol Biochem Biophys 36:1–252 PubMed DOI
Callan HG, Gall JG, Berg CA (1987) The lampbrush chromosomes of Xenopus laevis: preparation, identification, and distribution of 5S DNA sequences. Chromosoma 95:236–250 PubMed DOI
Chernyavskaya Y, Zhang X, Liu J, Blackburn J (2022) Long-read sequencing of the zebrafish genome reorganizes genomic architecture. BMC Genomics 23:116 PubMed DOI PMC
Daga RR, Thode G, Amores A (1996) Chromosome complement, C-banding, Ag-NOR and replication banding in the zebrafish Danio rerio. Chromosome Res 4:29–32 PubMed DOI
Daks AA, Deriusheva SE, Krasikova AV, Zlotina AM, Gaginskaia ER, Galkina SA (2010) Lampbrush chromosomes of the Japanese quail (Coturnix coturnix japonica): a new version of cytogenetic maps. Genetika 46:1335–1338 PubMed
Dedukh D, Mazepa G, Shabanov D, Rosanov J, Litvinchuk S, Borkin L, Saifitdinova A, Krasikova A (2013) Cytological maps of lampbrush chromosomes of European water frogs (Pelophylax esculentus complex) from the Eastern Ukraine. BMC Genet 14:26 PubMed DOI PMC
Dedukh D, Majtánová Z, Marta A, Pšenička M, Kotusz J, Klíma J, Juchno D, Boron A, Janko K (2020) Parthenogenesis as a solution to hybrid sterility: the mechanistic basis of meiotic distortions in clonal and sterile hybrids. Genetics 215:975–987 PubMed DOI PMC
Dedukh D, Da Cruz I, Kneitz S, Marta A, Ormanns J, Tichopád T, Lu Y, Alsheimer M, Janko K, Schartl M (2022) Achiasmatic meiosis in the unisexual Amazon molly, Poecilia Formosa. Chromosome Res 30(4):443–457 PubMed DOI
Dedukh D, Marta A, Myung RY, Ko MH, Choi DS, Won YJ, Janko K (2024) A cyclical switch of gametogenic pathways in hybrids depends on the ploidy level. Commun Biol 7(1):424 PubMed DOI PMC
Deng Z, Wang Z, Stong N, Plasschaert R, Moczan A, Chen H-S, Hu S, Wikramasinghe P, Davuluri RV, Bartolomei MS, Riethman H, Lieberman PM (2012) A role for CTCF and cohesin in subtelomere chromatin organization, TERRA transcription, and telomere end protection. EMBO J 31:4165–4178 PubMed DOI PMC
Deryusheva S, Krasikova A, Kulikova T, Gaginskaya E (2007) Tandem 41-bp repeats in chicken and Japanese quail genomes: FISH mapping and transcription analysis on lampbrush chromosomes. Chromosoma 116:519–530 PubMed DOI
Dosch R, Wagner DS, Mintzer KA, Runke G, Wiemelt AP, Mullins MC (2004) Maternal control of vertebrate development before the midblastula transition: mutants from the zebrafish I. Dev Cell 6:771–780 PubMed DOI
Ekker M, Fritz A, Westerfield M (1992) Identification of two families of satellite-like repetitive DNA sequences from the zebrafish (Brachydanio rerio). Genomics 13:1169–1173 PubMed DOI
Endo A, Ingalls TH (1968) Chromosomes of the zebra fish. A model for cytogenetic, embryologic, and ecologic study. J Hered 59:382–384 PubMed DOI
Epstein LM, Mahon KA, Gall JG (1986) Transcription of a satellite DNA in the newt. J Cell Biol 103:1137–1144 PubMed DOI
Freeman JL, Adeniyi A, Banerjee R, Dallaire S, Maguire SF, Chi J, Ng BL, Zepeda C, Scott CE, Humphray S, Rogers J, Zhou Y, Zon LI, Carter NP, Yang F, Lee C (2007) Definition of the zebrafish genome using flow cytometry and cytogenetic mapping. BMC Genomics 8:195 PubMed DOI PMC
Fukui K, Kato S (2021) Imaging approaches for chromosome structures. Chromosome Res 29:5–17 PubMed DOI
Gaginskaya E, Kulikova T, Krasikova A (2009) Avian lampbrush chromosomes: a powerful tool for exploration of genome expression. Cytogenet Genome Res 124:251–267 PubMed DOI
Galkina S, Deryusheva S, Fillon V, Vignal A, Crooijmans R, Groenen M, Rodionov A, Gaginskaya E (2006) FISH on avian lampbrush chromosomes produces higher resolution gene mapping. Genetica 128:241–251 PubMed DOI
Gall JG, Murphy C (1998) Assembly of lampbrush chromosomes from sperm chromatin. Mol Biol Cell 9:733–747 PubMed DOI PMC
Gall JG, Murphy C, Callan HG, Wu Z (1991) Chapter 8 Lampbrush chromosomes. In: Kay BK, Peng HB (eds) Methods in cell biology, Xenopus laevis: practical uses in cell and molecular biology. Academic Press, pp 149–166. https://doi.org/10.1016/S0091-679X(08)60276-9 DOI
Gall JG, Nizami ZF (2016) Isolation of giant lampbrush chromosomes from living oocytes of frogs and salamanders. J Vis Exp:e54103. https://doi.org/10.3791/54103
Gall JG (2014) Transcription in the Xenopus oocyte nucleus. In: Xenopus development. Wiley, pp 3–15. https://doi.org/10.1002/9781118492833.ch1
Gold JR (1974) A fast and easy method for chromosome karyotyping in adult teleosts. Progress Fish-Cult 36:169–171 DOI
Gornung E, Gabrielli I, Cataudella S, Sola L (1997) CMA3-banding pattern and fluorescence in situ hybridization with 18S rRNA genes in zebrafish chromosomes. Chromosome Res 5:40–46 PubMed DOI
Gornung E, Gabrielli I, Sola L (1998) Localization of the (TTAGGG)n telomeric sequence in zebrafish chromosomes. Genome 41(1):136–138 DOI
He L, Zhu Z, Faras AJ, Guise KS, Hackett PB, Kapuscinski AR (1992) Characterization of AluI repeats of zebrafish (Brachydanio rerio). Mol Mar Biol Biotechnol 1:125–135 PubMed
Howe K, Clark MD, Torroja CF, Torrance J, Berthelot C, Muffato M, Collins JE, Humphray S, McLaren K, Matthews L, McLaren S, Sealy I, Caccamo M, Churcher C, Scott C, Barrett JC, Koch R, Rauch G-J, White S et al (2013) The zebrafish reference genome sequence and its relationship to the human genome. Nature 496:498–503 PubMed DOI PMC
Idilli AI, Cusanelli E, Pagani F, Berardinelli F, Bernabé M, Cayuela ML, Poliani PL Mione MC (2020) Expression of tert prevents ALT in zebrafish brain tumors. Front Cell Dev Biol 8. https://doi.org/10.3389/fcell.2020.00065
Imai Y, Olaya I, Sakai N, Burgess SM (2021) Meiotic chromosome dynamics in zebrafish. Front Cell Dev Biol 9. https://doi.org/10.3389/fcell.2021.757445
Kishi S, Slack BE, Uchiyama J, Zhdanova IV (2009) Zebrafish as a genetic model in biological and behavioral gerontology: where development meets aging in vertebrates – a mini-review. Gerontology 55:430–441 PubMed DOI PMC
Kligerman AD, Bloom SE (1977) Rapid chromosome preparations from solid tissues of fishes. J Fish Res Board Can 34:266–269 DOI
Kossack ME, Draper BW (2019) Genetic regulation of sex determination and maintenance in zebrafish (Danio rerio). Curr Top Dev Biol 134:119–149 PubMed DOI PMC
Krasikova AV, Gaginskaia ER (2010) Organization of centromere regions of chromosomes in the lampbrush phase. Tsitologiia 52:515–533 PubMed
Krasikova A, Kulikova T (2019) Identification of genomic loci responsible for the formation of nuclear domains using lampbrush chromosomes. Non-Coding RNA 6:1 PubMed DOI PMC
Krasikova A, Kulikova T, Saifitdinova A, Derjusheva S, Gaginskaya E (2004) Centromeric protein bodies on avian lampbrush chromosomes contain a protein detectable with an antibody against DNA topoisomerase II. Chromosoma 113:316–323 PubMed DOI
Krasikova A, Barbero JL, Gaginskaya E (2005) Cohesion proteins are present in centromere protein bodies associated with avian lampbrush chromosomes. Chromosome Res 13:675–685 PubMed DOI
Krasikova A, Deryusheva S, Galkina S, Kurganova A, Evteev A, Gaginskaya E (2006) On the positions of centromeres in chicken lampbrush chromosomes. Chromosome Res 14:777–789 DOI
Krasikova AV, Vasilevskaya EV, Gaginskaya ER (2010) Chicken lampbrush chromosomes: transcription of tandemly repetitive DNA sequences. Russ J Genet 46:1173–1177 DOI
Krasikova A, Fukagawa T, Zlotina A (2012) High-resolution mapping and transcriptional activity analysis of chicken centromere sequences on giant lampbrush chromosomes. Chromosome Res 20:995–1008 PubMed DOI
Krasikova A, Fishman V, Kulikova T (2023a) Lampbrush chromosome studies in the post-genomic era. BioEssays 45:2200250 DOI
Krasikova A, Kulikova T, Rodriguez Ramos JS, Maslova A (2023b) Assignment of the somatic A/B compartments to chromatin domains in giant transcriptionally active lampbrush chromosomes. Epigenetics Chromatin 16:24 PubMed DOI PMC
Krasikova A, Kulikova T, Schelkunov M, Makarova N, Fedotova A, Plotnikov V, Berngardt V, Maslova A, Fedorov A (2024) The first chicken oocyte nucleus whole transcriptomic profile defines the spectrum of maternal mRNA and non-coding RNA genes transcribed by the lampbrush chromosomes. Nucleic Acids Res 52:12850–12877 https://doi.org/10.1093/nar/gkae941
Kulikova T, Chervyakova D, Zlotina A, Krasikova A, Gaginskaya E (2016) Giant poly(A)-rich RNP aggregates form at terminal regions of avian lampbrush chromosomes. Chromosoma 125:709–724 PubMed DOI
Kulikova T, Krasikova A (2022) RNA-FISH—on lampbrush chromosomes: visualization of individual transcription units. In: Cytogenetics and molecular cytogenetics. CRC Press, pp 307–317. https://doi.org/10.1201/9781003223658-26
Lerner EA, Lerner MR, Janeway CA, Steitz JA (1981) Monoclonal antibodies to nucleic acid-containing cellular constituents: probes for molecular biology and autoimmune disease. Proc Natl Acad Sci 78:2737–2741 PubMed DOI PMC
Li Y, Jia Z, Zhang S, He X (2021) Progress in gene-editing technology of zebrafish. Biomolecules 11:1300 PubMed DOI PMC
Lieschke GJ, Currie PD (2007) Animal models of human disease: zebrafish swim into view. Nat Rev Genet 8:353–367 PubMed DOI
Liew WC, Bartfai R, Lim Z, Sreenivasan R, Siegfried KR, Orban L (2012) Polygenic sex determination system in zebrafish. PLoS ONE 7:e34397 PubMed DOI PMC
Lin KW, Yan J (2008) Endings in the middle: current knowledge of interstitial telomeric sequences. Mutat Res 658:95–110 PubMed DOI
Macgregor HC, Varley JM, Morgan GT (1981) The transcription of satellite and ribosomal DNA sequences on lampbrush chromosomes of crested newts. In: Schweiger HG (ed) International cell biology 1980–1981. Springer, Berlin, pp 33–46
Macgregor HC, Sessions SK, Arntzen JW (1990) An integrative analysis of phylogenetic relationships among newts of the genus Triturus (family Salamandridae), using comparative biochemistry, cytogenetics and reproductive interactions. J Evol Biol 3:329–373 DOI
Marta A, Dedukh D, Bartoš O, Majtánová Z, Janko K (2020) Cytogenetic characterization of seven novel satDNA markers in two species of spined loaches (Cobitis) and their clonal hybrids. Genes 11:617 PubMed DOI PMC
Mayrhofer M, Gourain V, Reischl M, Affaticati P, Jenett A, Joly J-S, Benelli M, Demichelis F, Poliani PL, Sieger D, Mione M (2017) A novel brain tumour model in zebrafish reveals the role of YAP activation in MAPK- and PI3K-induced malignant growth. Dis Model Mech 10:15–28 PubMed PMC
Miura I, Ohtani H, Hanada H, Ichikawa Y, Kashiwagi A, Nakamura M (1997) Evidence for two successive pericentric inversions in sex lampbrush chromosomes of Rana rugosa (Anura: Ranidae). Chromosoma 106:178–182 PubMed DOI
Moens PB (2006) Zebrafish: chiasmata and interference. Genome 49:205–208 PubMed DOI
Morgan GT (2002) Lampbrush chromosomes and associated bodies: new insights into principles of nuclear structure and function. Chromosome Res 10:177–200 PubMed DOI
Nizami Z, Deryusheva S, Gall JG (2010) The Cajal body and histone locus body. Cold Spring Harb Perspect Biol 2:a000653 PubMed DOI PMC
NRC (2010) Guide for the care and use of laboratory animals, 8th edn. National Academies Press, Washington
Ortega-Recalde O, Day RC, Gemmell NJ, Hore TA (2019) Zebrafish preserve global germline DNA methylation while sex-linked rDNA is amplified and demethylated during feminisation. Nat Commun 10:3053 PubMed DOI PMC
Penrad-Mobayed M, El Jamil A, Kanhoush R, Perrin C (2009) Working map of the lampbrush chromosomes of Xenopus tropicalis: a new tool for cytogenetic analyses. Dev Dyn off Publ Am Assoc Anat 238:1492–1501
Penrad-Mobayed M, Perrin C, Lepesant JA (2012) Precocious detection on amphibian oocyte lampbrush chromosomes of subtle changes in the cellular localisation of the Ro52 protein induced by in vitro culture. Chromosome Res 20:1033–1044 PubMed DOI
Phillips RB, Reed KM (2000) Localization of repetitive DNAs to zebrafish (Danio rerio) chromosomes by fluorescence in situ hybridization (FISH). Chromosome Res 8:27–35 PubMed DOI
Phillips RB, Amores A, Morasch MR, Wilson C, Postlethwait JH (2006) Assignment of zebrafish genetic linkage groups to chromosomes. Cytogenet Genome Res 114:155–162 PubMed DOI
Pijnacker LP, Ferwerda MA (1995) Zebrafish chromosome banding. Genome 38:1052–1055 PubMed DOI
Schindelin J, Rueden CT, Hiner MC, Eliceiri KW (2015) The ImageJ ecosystem: an open platform for biomedical image analysis. Mol Reprod Dev 82(7–8):518–529 PubMed DOI PMC
Schoeftner S, Blasco MA (2008) Developmentally regulated transcription of mammalian telomeres by DNA-dependent RNA polymerase II. Nat Cell Biol 10:228–236 PubMed DOI
Sharma KK, Sharma OP, Tripathi NK, Sharma KK, Sharma OP, Tripathi NK (1998) Female heterogamety in Danio rerio (Cypriniformes: Cyprinidae). Proc Natl Acad Sci India Sect B Biol Sci 68:123–126
Smurova K, De Wulf P (2018) Centromere and pericentromere transcription: roles and regulation in sickness and in health. Front Genet 9:674 PubMed DOI PMC
Sola L, Gornung E (2001) Classical and molecular cytogenetics of the zebrafish, Danio rerio (Cyprinidae, Cypriniformes): an overview. Genetica 111:397–412 PubMed DOI
Solovei I, Gaginskaya ER, Macgregor HC (1994) The arrangement and transcription of telomere DNA sequences at the ends of lampbrush chromosomes of birds. Chromosome Res 2:460–470 PubMed DOI
Solovei I, Ogawa A, Naito M, Mizuno S, Macgregor H (1998) Specific chromomeres on the chicken W lampbrush chromosome contain specific repetitive DNA sequence families. Chromosome Res 6:323–327 PubMed DOI
Solovei I, MacGregor HC, Gaginskaia ER (1995) Specifically terminal clusters of telomere DNA sequences are transcribed from the C-rich strand on chicken lampbrush chromosomes. In: Brandham PF, Bennet MD (eds) Presented at the Proceedings of Kew Chromosome Conference IV. Royal Botanic Gardens (KRBG), Richmond, pp 323–330
Spence R, Gerlach G, Lawrence C, Smith C (2008) The behaviour and ecology of the zebrafish, Danio rerio. Biol Rev Camb Philos Soc 83:13–34 PubMed DOI
Trofimova I, Krasikova A (2016) Transcription of highly repetitive tandemly organized DNA in amphibians and birds: a historical overview and modern concepts. RNA Biol 13:1246–1257 PubMed DOI PMC
Vesterlund L, Jiao H, Unneberg P, Hovatta O, Kere J (2011) The zebrafish transcriptome during early development. BMC Dev Biol 11:30 PubMed DOI PMC
Wallace BMN, Wallace H (2003) Synaptonemal complex karyotype of zebrafish. Heredity 90:136–140 PubMed DOI
Wei C, Salichos L, Wittgrove CM, Rokas A, Patton JG (2012) Transcriptome-wide analysis of small RNA expression in early zebrafish development. RNA 18:915–929 PubMed DOI PMC
Whiteley AR, Bhat A, Martins EP, Mayden RL, Arunachalam M, Uusi-Heikkilä S, Ahmed ATA, Shrestha J, Clark M, Stemple D, Bernatchez L (2011) Population genomics of wild and laboratory zebrafish (Danio rerio). Mol Ecol 20:4259–4276 PubMed DOI PMC
Wilson CA, High SK, McCluskey BM, Amores A, Yan Y, Titus TA, Anderson JL, Batzel P, Carvan MJ, Schartl M, Postlethwait JH (2014) Wild sex in zebrafish: loss of the natural sex determinant in domesticated strains. Genetics 198:1291–1308 PubMed DOI PMC
Wu Z, Murphy C, Gall JG (1994) Human p80-coilin is targeted to sphere organelles in the amphibian germinal vesicle. Mol Biol Cell 5:1119–1127 PubMed DOI PMC
Yang H, Luan Y, Liu T, Lee HJ, Fang L, Wang Y, Wang X, Zhang B, Jin Q, Ang KC, Xing X, Wang J, Xu J, Song F, Sriranga I, Khunsriraksakul C, Salameh T, Li D, Choudhary MNK, Topczewski J, Wang K, Gerhard GS, Hardison RC, Wang T, Cheng KC, Yue F (2020) A map of cis-regulatory elements and 3D genome structures in zebrafish. Nature 588:337–343 PubMed DOI PMC
Zlotina A, Krasikova A (2017) FISH in lampbrush chromosomes. In: Liehr T (ed) Fluorescence in situ hybridization (FISH): application guide. Springer, Berlin, pp 445–457 DOI
Zlotina A, Dedukh D, Krasikova A (2017) Amphibian and avian karyotype evolution: insights from lampbrush chromosome studies. Genes 8:311 PubMed DOI PMC