The First and Current Checklist of the Animal Species Bearing Lampbrush Chromosomes

Nadim Yılmazer; Melek Keskin Başpınar

doi:10.35229/jaes.1667709

TR EN

İlk ve Güncel Lamba Fırçası Kromozomları Taşıyan Hayvan Türleri Listesi

Öz

Hemen hemen tüm hayvan türlerinde, yumurta hücreleri embriyo oluşumunu desteklemek amacıyla somatik hücrelere kıyasla belirgin bir boyut farkı gösterir. Yumurtaların hızlı ve bol miktarda üretilmesi genellikle özel mekanizmalar gerektirir. Bu mekanizmalardan biri, çekirdek hacmi ve kromozomlarda transkripsiyon aktivitesi artışı ile karakterize edilen diploten arrestidir; bu süreçte, belirgin lamba fırçası kromozomları ortaya çıkar. Oldukça uzun yapıya sahip olan lamba fırçası kromozomları, çekirdekten izole edilmelerinin kolay olması nedeniyle en iyi amfibilerde ve kuşlarda incelenmiştir. Mart 2025’e kadar elektronik veri tabanları taranarak yapılan kapsamlı bilimsel literatür incelemesi, 31’i omurgasız ve 166’sı omurgalı olmak üzere toplamda 197 hayvan türünde lamba fırçası kromozomlarının varlığını ortaya koymuştur. Bu kromozomların böylesine geniş ve çeşitli hayvan türlerinde görülmesi, yumurta büyümesi için bu mekanizmanın eski bir evrimsel kökene sahip olduğunu düşündürmektedir.

Anahtar Kelimeler

Diploten arresti , omurgalılar , omurgasızlar , ovogenez , oogenez , yumurta büyümesi

The First and Current Checklist of the Animal Species Bearing Lampbrush Chromosomes

Abstract

In virtually all animal species, egg cells exhibit a notable size disparity compared to somatic cells in order to support the production of an embryo. The rapid and voluminous production of eggs, often in abundance, necessitates specialized mechanisms. Among these mechanisms is diplotene arrest, a stage characterized by nuclear expansion and heightened chromosomal transcriptional activity, resulting in the formation of distinct lampbrush chromosomes. Remarkably long chromosomes, lampbrush chromosomes have been best studied in amphibians and birds due to their ease of isolation from the nucleus. A thorough review of scientific literature conducted until March 2025 across electronic databases unveiled the presence of lampbrush chromosomes in a total of 197 animal species, encompassing 31 invertebrates and 166 vertebrates. The widespread occurrence of lampbrush chromosomes across such a diverse array of animal species suggests an ancient evolutionary origin for this mechanism of egg growth.

Keywords

Diploten arrest , egg growth , invertebrates , oogenesis , vertebrates

Kaynakça

Akhi, F.J., Haque, S.M., Miah, M.I., & Haque, M.A. (2024). Ovarian histology of the freshwater catfish Silonia silondia (Hamilton, 1822). Heliyon, 10, e33812. DOI: 10.1016/j.heliyon.2024.e33812
Al-Amri, I.S.S. (2012). Reproductive cycle of the house gecko, Hemidactylus flaviviridis, in Oman in relation to morphological and ultrastructural changes and plasma steroid concentrations with reference to localisation of progesterone receptors. Ph.D. Dissertation, University of Portsmouth, 375p.
Angelier, N., Penrad-Mobayed, M., Billoud, B., Bonnanfant-Jaïs, M.L., & Coumailleau, P. (1996). What role might lampbrush chromosomes play in maternal gene expression?. Int J Dev Biol, 40, 645-652.
Arronet, V.N. (1973). Morphological changes of nuclear structures in the oogenesis of reptiles (Lacertidae, Agamidae). J Herpetol, 7, 163-193. DOI: 10.2307/1563001
Bara, G. (1960). Histological and cytological change in the ovaries of mackerel Scomber scomber L. during the annual cycle. Istanbul Univ Fen Fak Mecm Ser B, 25, 49-91.
Barsacchi, G., Bussoti, L., & Mancino, G. (1970). The maps of the lampbrush chromosomes of Triturus (Amphibia Urodela). IV. Triturus vulgaris meridionalis. Chromosoma, 31, 255-270. DOI: 10.1007/BF00321223
Baumeister, H.G. (1973). Lampbrush chromosomes and RNA-synthesis during early oogenesis of Brachydanio rerio (Cyprinidae, Teleostei). Z Zellforsch Mikrosk Anat, 145, 145-150. DOI: 10.1007/BF00307195
Berthelin, C., Dubroca, L., Kellner, K., Le Meleder, A., Martin, V., & Sauger, C. (2022). Lexicon of histological structures found in the ovaries and during the oogenesis of the red mullet, Mullus surmuletus (Linnaeus, 1758). Archimer, DOI: 10.13155/75174
Bi, K., & Bogart, J.P. (2010). Probing the meiotic mechanism of intergenomic exchanges by genomic in situ hybridization on lampbrush chromosomes of unisexual Ambystoma (Amphibia: Caudata). Chromosome Res., 18, 371- 382. DOI: 10.1007/s10577-010-9121-3
Bier, K., Kunz, W., & Ribbert, D. (1967). Structure and function of oocyte chromosomes and nucleoli, as well as extra-DNA during oogenesis in panoistic and meroistic insects. Chromosoma, 23, 214-254. DOI: 10.1007/BF00331114

Bogart, J.P. (2003). Genetics and systematics of hybrid species, In: Sever DM (Ed), Reproductive Biology and Phylogeny of Urodela, 1st ed., 109-134p, CRC Press, Florida.
Bottke, W. (1973). Lampbrush chromosomes and amphinucleoli in oocyte nuclei of the snail Bithynia tentaculata L. Chromosoma, 42, 175- 190. DOI: 10.1007/BF00320939
Boyd, M.M.M. (1940). The structure of the ovary and the formation of the corpus luteum in Hoplodactylus maculatus, Gray. Q J Microsc Sci, 82, 337-376. DOI: 10.1242/jcs.s2-82.326.337
Bucci-Innocenti, S., Ragghianti, M., & Mancino, G. (1983). Investigations of karyology and hybrids in Triturus boscai and T. vittatus, with a reinterpretation of the species groups within Triturus (Caudata: Salamandridae). Copeia, 3, 662-672. DOI: 10.2307/1444330
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 Suppl, 255, 37-56. DOI: 10.1002/jez.1402550107
Callan, H.G. (1957). The lampbrush chromosomes of Sepia officinalis L., Anilocra physodes L. and Scyllium catulus Cuv. and their structural relationship to the lampbrush chromosomes of Amphibia. Pubbl Stn Zool Napoli, 29, 329-346.
Callan, H.G., & Lloyd, L. (1960). Lampbrush chromosomes of crested newts Triturus cristatus (Laurenti). Philos. Trans. R. Soc. B: Biol. Sci., 243, 135-219. DOI: 10.1098/rstb.1960.0007
Callan, H.G. (1966). Chromosomes and nucleoli of the axolotl, Ambystoma mexicanum. J. Cell Sci., 1, 85-108. DOI: 10.1242/jcs.1.1.85 Callan, H.G. (1986). Lampbrush Chromosomes, Springer, Berlin, 256p.
Callebaut, M., Van Nassauw, L., & Harrisson, F. (1997). Comparison between oogenesis and related ovarian structures in a reptile, Pseudemys scripta elegans (turtle) and in a bird Coturnix coturnix japonica (quail). Reprod Nutr. Dev., 37, 233-252. DOI: 10.1051/rnd:19970301
Coimbra, A., & Azevedo, C. (1984). Structure and evolution of the nucleolus during oogenesis, In: Van Blerkom J, Motta PM (Eds), Ultrastructure of Reproduction- Gametogenesis, Fertilization, and Embryogenesis. Electron Microscopy in Biology and Medicine (Current Topics in Ultrastructural Research), Vol 2, 127-139p, Boston Springer. DOI: 10.1007/978-1-4613- 3867-3_11
Davidian, A., Koshel, E., Dyomin, A., Galkina, S., Saifitdinova, A., & Gaginskaya, E. (2021). On some structural and evolutionary aspects of rDNA amplification in oogenesis of Trachemys scripta turtles. Cell Tissue Res., 383, 853-864. DOI: 10.1007/s00441-020-03282-x
Davidson, E.H., & Hough, B.R. (1969). Synchronous oogenesis in Engystomops pustulosus, a neotropic anuran suitable for laboratory studies: localization in the embryo of RNA synthesized at the lampbrush stage. J. Exp. Zool., 172, 25-48. DOI: 10.1002/jez.1401720104
Davidson, E.H. (1986). Gene Activity in Early Development, Academic Press, Florida, 670p. Dävring, L., & Sunner, M. (1982). A lampbrush phase in oocytes of Drosophila and its bearing upon mutagen sensitivity data. Hereditas, 97, 247-259. DOI: 10.1111/j.1601-5223.1982.tb00878.x
Dävring, L. (1983). Lampbrush chromosomes in the meroistic ovaries of the blowfly Calliphora erythrocephala. Hereditas, 99, 177-185. DOI: 10.1111/j.1601-5223.1983.tb00889.x
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. DOI: 10.1186/1471-2156-14-26
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, 443-457. DOI: 10.1007/s10577-022-09708-2
Dedukh, D., Marta, A., Myung, R.Y., Ko, M.H., Choi, D.S., Won, Y.J., & Janko, K. (2024a). A cyclical switch of gametogenic pathways in hybrids depends on the ploidy level. Commun Biol., 7, 424. DOI: 10.1038/s42003-024-05948-6
Dedukh, D., Lisachov, A., Panthum, T., Singchat, W., Matsuda, Y., Imai, Y., Janko, K., & Srikulnath, K. (2024b). Meiotic deviations and endoreplication lead to diploid oocytes in female hybrids between bighead catfish (Clarias macrocephalus) and North African catfish (Clarias gariepinus). Front Cell Dev Biol, 12, 1465335. DOI: 10.3389/fcell.2024.1465335
Dedukh, D., Kulikova, T., Dobrovolskaia, M., Maslova, A., & Krasikova, A. (2025). Lampbrush chromosomes of Danio rerio. Chromosome Res., 33, 2. DOI: 10.1007/s10577-024-09761-z
Delobel, N., & Delavault, R. (1971). Lampbrush chromosomes in Echinaster sepositus (Echinoderm, Asteroid). Caryologia, 24, 251- 259. DOI: 10.1080/00087114.1971.10796433
Derdak, A., Jędrzejowska, I., & Mąkol, J. (2024). The ovary structure in terrestrial parasitengona mites: The case of Trombidiidae (Acariformes: Parasitengona). J. Morphol., 285, e21774. DOI: 10.1002/jmor.21774
Domínguez-Castanedo, O., Hernandez-Coronado, C.G., Martínez-Espinosa, D.A. & Rosales- Torres, A.M. (2024). Reproductive morphophysiology of an iteroparous batch spawner fish: from early follicle development to ovulation. J. Fish Biol., 105, 1298-1313. DOI: 10.1111/jfb.15891
Dudzik, A., Dedukh, D., Crochet, P.A., Rozenblut- Kościsty, B., Rybka, H., Doniol-Valcroze, P., Choleva, L., Ogielska, M., & Chmielewska, M. (2023). Cytogenetics of the hybridogenetic frog Pelophylax grafi and its parental species Pelophylax perezi. Genome Biol Evol, 15, evad215. DOI: 10.1093/gbe/evad215
Fabergé, A.C. (1970). A doublet structure in the loops of lampbrush chromosomes of the newt, Taricha granulosa. Caryologia, 23, 241-250.
Fuentes, S.N., Awruch, C.A., Moya, C., Wehitt, A., & Díaz Andrade, M.C. (2023). First detailed description of follicle development in a chimaeroid, the American elephant fish Callorhinchus callorynchus. Theriogenology Wild, 2, 100037. DOI: 10.1016/j.therwi.2023.100037
Gaginskaya, E.R. (1972). The nuclear structures in oocytes of adult birds. I. Chromosome behaviour during the oocyte cytoplasm growth. Tsitologiia, 14, 426-432.
Gall, J.G. (1954). Lampbrush chromosomes from oocyte nuclei of the newt. J Morphol, 94, 283-351. DOI: 10.1002/jmor.1050940203
García-Valdez, V., Sánchez-Loria, O.L., & Chamut, S. (2019). Oogenesis and ovarian histology of the South American lizard Salvator merianae. Rev Agron Noroeste Argent, 39, 141-154.
Giorgi, F., & Galleni, L. (1972). The lampbrush chromosomes of Rana esculenta L. (Amphibia- Anura). Caryologia, 25, 107-123. DOI: 10.1080/00087114.1972.10796470
Guerrini, F., Bucci, S., Ragghianti, M., Mancino, G., Hotz, H., Uzzell, T., & Berger, L. (1997). Genomes of two water frog species resist germ line exclusion in interspecies hybrids. J Exp Zool, 279, 163-176. DOI: 10.1002/(sici)1097- 010x(19971001)279:2<163::aid-jez7>3.0.co;2-m Guraya, S.S. (1989). Ovarian Follicles in Reptiles and Birds, Springer, Berlin, 285p.
Hei, N., Yang, P., Yang, Y., Liu, J., Bao, H., Liu, H., Zhang, H., & Chen, Q. (2010). Fine structural observation on the oogenesis and vitellogenesis of the Chinese soft-shelled turtle (Pelodiseus sinensis). Zygote, 18, 109-120. DOI: 10.1017/S0967199409990116
Hernández-Franyutti, A., Uribe Aranzábal, M.C., & Guillette, L.J. Jr. (2005). Oogenesis in the viviparous matrotrophic lizard Mabuya brachypoda. J Morphol, 265, 152-164. DOI: 10.1002/jmor.10347
Ibrahim, M.M., & Wilson, I.B. (1989). Light and electron microscope studies on ovarian follicles in the lizard Chalcides ocellatus. J. Zool., 218, 187-208. DOI: 10.1111/j.1469-7998.1989.tb02532.x
Iegorova, V., Naraine, R., Psenicka, M., Zelazowska, M. & Sindelka, R. (2022). Comparison of RNA localization during oogenesis within Acipenser ruthenus and Xenopus laevis. Front Cell Dev. Biol., 10, 982732. DOI: 10.3389/fcell.2022.982732
Ikebe, C., Kuro-o, M., Ohtani, H., Kawase, Y., Matsui, T., & Kohno, S. (2005). Cytogenetic studies of Hynobiidae (Urodela) XIX. Morphological variation of sex chromosomes pairing behavior of sex lampbrush chromosomes in Hynobius quelpaertensis (Mori) from Cheju Island, South Korea. Chromosome Res., 13, 157-167. DOI: 10.1007/s10577-005-8036-x
Imoh, H. (1981). Changes in nucleoli at maturation of newt oocyte. Dev Growth Differ, 23, 33-39. DOI: 0.1111/j.1440-169X.1981.00033.x
Jessus, C., Munro, C., & Houliston, E. (2020). Managing the oocyte meiotic arrest - lessons from frogs and jellyfish. Cells, 9, 1150. DOI: 10.3390/cells9051150
Keinath, M.C., Davidian, A., Timoshevskiy, V., Timoshevskaya, N. & Gall, J.G. (2021). Characterization of axolotl lampbrush chromosomes by fluorescence in situ hybridization and immunostaining. Exp. Cell Res., 401, 112523. DOI: 10.1016/j.yexcr.2021.112523
Kellner, K., Sauger, C., & Berthelin, C. (2024a). Lexicon of histological structures found in the ovaries and during the oogenesis of the megrim, Lepidorhombus whiffiagonis (Walbaum, 1792). HAL hal-04732902. DOI: 10.13155/75170
Kellner, K., Berthelin, C., & Sauger, C. (2024b). Lexicon of histological structures found in the ovaries and during the oogenesis of the four-spot megrim, Lepidorhombus boscii (Risso, 1810). HAL hal-04732944. DOI: 10.13155/74844
Kezer, J., & Macgregor, H.C. (1973). The nucleolar organizer of Plethodon cinereus cinereus (Green). II. The lampbrush nucleolar organizer. Chromosoma, 42, 427-444. DOI: 10.1007/BF00399410
Kezer, J., León, P.E., & Sessions, S.K. (1980). Structural differentiation of the meiotic and mitotic chromosomes of the salamander, Ambystoma macrodactylum. Chromosoma, 81, 177-197. DOI: 10.1007/BF00285948
King, H.D. (1908). The oogenesis of Bufo lentiginosus. J. Morphol., 19, 369-438. DOI: 10.1002/jmor.1050190202
Koshel, E., Galkina, S., Saifitdinova, A., Dyomin, A., Deryusheva, S., & Gaginskaya, E. (2016). Ribosomal RNA gene functioning in avian oogenesis. Cell Tissue Res., 366, 533-542. DOI: 10.1007/s00441-016-2444-4
Kulikova, T., Surkova, A., Zlotina, A., & Krasikova, A. (2020). Mapping epigenetic modifications on chicken lampbrush chromosomes. Mol. Cytogenet., 13, 32. DOI: 10.1186/s13039-020- 00496-0
Kunz, W. (1967a). Functional structures in the oocyte nucleus of Locusta migratoria. Chromosoma, 20, 332-370. DOI: 10.1007/BF00326189
Kunz, W. (1967b). Lampbrush chromosomes and multiple nucleoli in orthopterans. Chromosoma, 21, 446- 462. DOI: 10.1007/BF00336952
Kunz, W. (1969). The origin of multiple oocyte nucleoli from accessory DNA bodies in Gryllus domesticus. Chromosoma, 26, 41-75. DOI: 10.1007/BF00319499
Kupriyanova, L., & Safronova, L. (2023). A brief review of meiotic chromosomes in early spermatogenesis and oogenesis and mitotic chromosomes in the viviparous lizard Zootoca vivipara (Squamata: Lacertidae) with multiple sex chromosomes. Animals, 13, 19. DOI: 10.3390/ani13010019
Lacroix, J.C. (1968). Descriptive study of lampbrush chromosomes in the genus Pleurodeles (Amphibian, Urodele). Ann Embr Morph, 1, 179- 202.
Lafontaine, J.G., & Ris, H. (1958). An electron microscope study of lampbrush chromosomes. J. Biophys. Biochem. Cytol., 4, 99-106. DOI: 10.1083/jcb.4.1.99
Leon, P.E., & Kezer, J. (1974). The chromosomes of Siren intermedia nettingi (Goin) and their significance to comparative salamander karyology. Herpetologica, 30, 1-11.
Lukina, N.A. (1994). Characterization of meiotic chromosomes in the oocytes of some Lacertidae (Reptilia). Tsitologiia, 36, 323-329.
Macgregor, H.C., & Uzzell, T.M. Jr. (1964). Gynogenesis in salamanders related to Ambystoma jeffersonianum. Science, 143, 1043- 1045. DOI: 10.1126/science.143.3610.1043
Macgregor, H.C., & Kezer, J. (1970). Gene amplification in oocytes with 8 germinal vesicles from the tailed frog Ascaphus truei Stejneger. Chromosoma, 29, 189-206. DOI: 10.1007/BF00326078
Macgregor, H., & Klosterman, L. (1979). Observations on the cytology of Bipes (Amphisbaenia) with special reference to its lampbrush chromosomes. Chromosoma, 72, 67-87. DOI: 10.1007/BF00286430
Macgregor, H. (1980). Recent developments in the study of lampbrush chromosomes. Heredity, 44, 3-35. DOI: 10.1038/hdy.1980.2
Macgregor, H.C., & del Pino, E. (1982). Ribosomal gene amplification in multinucleate oocytes of the egg brooding hylid frog Flectonotus pygmaeus. Chromosoma, 85, 475-488. DOI: 10.1007/BF00327344
Macgregor, H.C. (1984). Lampbrush chromosomes and gene utilization in meiotic prophase. Symp. Soc. Exp. Biol., 38, 333-347.
Macgregor, H.C., Sessions, S.K., & Arntzen, J.W. (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: 10.1046/j.1420-9101.1990.3050329.x
Machado-Santos, C., Santana, L.N.S., Vargas, R.F., Abidu-Figueiredo, M., Brito-Gitirana, L., & Chagas, M.A. (2015). Histological and immunohistochemical study of the ovaries and oviducts of the juvenile female of Caiman latirostris (Crocodilia: Alligatoridae). Zoologia, 32, 395-402. DOI: 10.1590/S1984- 46702015000500008
Mancino, G., & Barsacchi, G. (1966). The maps of lampbrush chromosomes of Triturus (Urodele Amphibians). II. Triturus helveticus helveticus. Rivista di Biologia (Perugia), 59, 311-351.
Mancino, G., & Barsacchi, G. (1969). The maps of the lampbrush chromosomes of Triturus (Amphibia Urodela). III. Triturus italicus. Ann Embryol Morphog, 2, 355-377.
Mancino, G., Barsacchi, G., & Nardi, I. (1969). The lamphbrush chromosomes of Salamandra salamandra (L.) (Amphibia Urodela). Chromosoma, 26, 365-387. DOI: 10.1007/BF00326350
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. DOI: 10.3390/genes11060617
Masui, Y. (2001). From oocyte maturation to the in vitro cell cycle: the history of discoveries of Maturation-Promoting Factor (MPF) and Cytostatic Factor (CSF). Differentiation, 69, 1-17. DOI: 10.1046/j.1432-0436.2001.690101.x
Mishin, V.L. (1980). Interrelation between the sexual and digestive systems of chaetognaths (Chaetognatha). Arkhiv Anatomii Gistologii i émbriologii, 79, 63-67.
Miura, I., Ohtani, H., Kashiwagi, A., Hanada, H., & Nakamura, M. (1996). Structural differences between XX and ZW sex lampbrush chromosomes in Rana rugosa females (Anura: Ranidae). Chromosoma, 105, 237-241. DOI: 10.1007/BF02528772
Moiseeva, E., Rabinowitz, C., Paz, G., & Rinkevich, B. (2017). Histological study on maturation, fertilization and the state of gonadal region following spawning in the model sea anemone, Nematostella vectensis. PLoS ONE, 12, e0182677. DOI: 10.1371/journal.pone.0182677
Montezol, M., Cassel, M., Silva, D., Ferreira, A., & Mehanna, M. (2018). Gametogenesis and reproductive dynamics of Rhinella schneideri (Anura: Bufonidae): Influence of environmental and anthropogenic factors. Acta Zool, 99, 93-104. DOI: 10.1111/azo.12195
Müller, W.P. (1974). The lampbrush chromosomes of Xenopus laevis (Daudin). Chromosoma, 47, 283- 296. DOI: 10.1007/BF00328862
Nardi, I., Ragghianti, M., & Mancino, G. (1972). Characterization of the lampbrush chromosomes of the marbled newt Triturus marmoratus (Latreille, 1800). Chromosoma, 37, 1-22. DOI: 10.1007/BF00329554
Nie, H., Xu, Y., Zhang, Y., Wen, Y., Zhan, J., Xia, Y., Zhou, Y., Wang, R., & Wu, X. (2023). The effects of endogenous FSH and its receptor on oogenesis and folliculogenesis in female Alligator sinensis. BMC Zool., 8, 8. DOI: 10.1186/s40850- 023-00170-z
Ohtani, H. (1990). Lampbrush chromosomes of Rana nigromaculata, R. brevipoda, R. plancyi chosenia, R. p. fukienensis and their reciprocal hybrids. Scientific Report of the Laboratory for Amphibian Biology, Hiroshima University, 10, 165-221.
Ohtani, H. (1995). Local variations in the lampbrush chromosomes of the Japanese pond frog, Rana porosa. Caryologia, 48, 189-199. DOI: 10.1080/00087114.1995.10797329
Omar, D.C. (2024). Ovarian structure and oogenesis of two endemic pupfishes from the Yucatán Peninsula: morphofunctional traits related with an estuarine life history. Zoomorphology, 143, 443- 458. DOI: 10.1007/s00435-024-00653-8
Paschoal, L.R.P., & Zara, F.J. (2023). Assessing the ovarian development of Macrobrachium amazonicum (Heller, 1862) phenotypes by means of an integrative analysis. Tissue Cell, 84, 102166. DOI: 10.1016/j.tice.2023.102166
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. Dynam., 238, 1492-1501. DOI: 10.1002/dvdy.21930
Porceddu, R., Porcu, C., Mulas, G., Spiga, S., & Follesa, M.C. (2024). Ontogenetic changes in the tyrosine hydroxylase immunoreactive preoptic area in the small-spotted catshark Scyliorhinus canicula (L., 1758) females: catecholaminergic involvement in sexual maturation. Front Neuroanat, 17, 1301651. DOI: 10.3389/fnana.2023.1301651
Ragghianti, M., Nardi, I., & Mancino, G. (1972). Completion of the morphology of the lampbrush chromosomes of the Italian Alpine newt Triturus alpestris apuanus Bonaparte. Experientia (Basel), 28, 588-590. DOI: 10.1007/BF01931895
Ragghianti, M., Bucci-Innocenti, S., & Mancino, G. (1978). Karyology of the Carpathian newt Triturus montandoni and cytotaxonomic considerations on the species group T. vulgaris (Urodela: Salamandridae). Caryologia, 31, 243- 256. DOI: 10.1080/00087114.1978.10796748
Rogers, R.E., & Browder, L.W. (1977). Morphological observations on cultured lampbrush-stage Rana pipiens oocytes. Dev. Biol., 55, 135-147. DOI: 10.1016/0012-1606(77)90325-6
Saifitdinova, A.F., Galkina, S.A., & Gaginskaya, E.R. (2021). The Evolution of concepts about the biological role of lampbrush chromosomes. Russ. J. Genet., 57, 499-514. DOI: 10.1134/S1022795421050100
Sauger, C., Quinquis, J., Berthelin, C., Lepoittevin, M., Elie, N., Dubroca, L., & Kellner, K.A. (2023). Quantitative histologic analysis of oogenesis in the flatfish Species Pleuronectes platessa as a tool for fisheries management. Animals, 13, 2506. DOI: 10.3390/ani13152506
Solovei, I., Gaginskaya, E., Hutchison, N., & Macgregor, H. (1993). Avian sex chromosomes in the lampbrush form: the ZW lampbrush bivalents from six species of bird. Chromosome Res., 1, 153-166. DOI: 10.1007/BF00710769
Srivastava, M.D.L., & Bhatnagar, A.N. (1962). Lampbrush chromosomes of Rana cyanophlyctis. Cytologia, 27, 60-71. DOI: 10.1007/BF00710769
Stille, B., & Dävring, L. (1980). Meiosis and reproductive strategy in the parthenogenetic gall wasp Diplolepis rosae (L.) (Hymenoptera, Cynipidae). Hereditas, 92, 353-362. DOI: 10.1111/j.1601- 5223.1980.tb01720.x
Sumner, A.T. (2003). Chromosomes: organization and function, Blackwell Science Ltd., Oxford, 304p.
Torgasheva, A.A., Malinovskaya, L.P., Zadesenets, K.S., Karamysheva, T.V., Kizilova, E.A., Akberdina, E.A. et al. (2019). Germline- restricted chromosome (GRC) is widespread among songbirds. Proc Natl Acad Sci USA, 116, 11650-11845. DOI: 10.1073/pnas.1817373116
Tsvetkov, A.G., & Parfenov, V.N. (1994). Seasonal transformations in the lampbrush chromosomes and the morphogenesis of the karyosphere capsule in Rana temporaria oocytes detectable by an analysis of the isolated nuclear structures. Tsitologiia, 36, 64-70.
Tworzydlo, W., Marek, M., & Kisiel, E. (2017). Meiosis, Balbiani body and early asymmetry of Thermobia oocyte. Protoplasma, 254, 649-655. DOI: 10.1007/s00709-016-0978-7
Ullerich, F.H. (1970). DNA content and chromosome structure in amphibians. Chromosoma, 30, 1-37. DOI: 10.1007/BF00293907
Uribe, M.D.C.A., Omana, M.E.M., Quintero, J.G., & Guillette, L.J. Jr. (1995). Seasonal variation in ovarian histology of the viviparous lizard Sceloporus torquatus torquatus. J. Morphol., 226, 103-119. DOI: 10.1002/jmor.1052260107
Uribe, M.C.A., & Guillette, L.J. Jr. (2000). Oogenesis and ovarian histology of the American alligator Alligator mississippiensis. J Morphol, 245, 225- 240. DOI: 10.1002/1097- 4687(200009)245:3<225::AID- JMOR4>3.0.CO;2-M
Uribe, M.C., & Grier, H.J. (2011). Oogenesis of microlecithal oocytes in the viviparous teleost Heterandria formosa. J Morphol, 272, 241-57. DOI: 10.1002/jmor.10912
Wallace, R.A., & Selman, K. (1981). Cellular and dynamic aspects of oocyte growth in teleosts. Am Zool, 21, 325-343. DOI: 10.1093/icb/21.2.325
Wang, X., & Pepling, M.E. (2021). Regulation of meiotic prophase one in mammalian oocytes. Front Cell Dev. Bio.l, 9, 667306. DOI: 10.3389/fcell.2021.667306
Weith, A., & Traut, W. (1980). Synaptonemal complexes with associated chromatin in a moth, Ephestia kuehniella Z. The fine structure of the W chromosomal heterochromatin. Chromosoma, 78, 275-291. DOI: 10.1007/BF00327388
Wu, Z., Murphy, C., & Gall, J.G. (1986). A transcribed satellite DNA from the bullfrog Rana catesbeiana. Chromosoma, 93, 291-297. DOI: 10.1007/BF00327586
Żelazowska, M., & Halajian, A. (2019). Previtellogenic oocytes of South African largemouth bass Micropterus salmoides Lacépède 1802 (Actinopterygii, Perciformes) - the Balbiani body, cortical alveoli and developing eggshell. J. Morphol., 280, 360-369. DOI: 10.1002/jmor.20948
Żelazowska, M., & Halajian, A. (2020). Asymmetry in the cytoplasm of oocytes of largescale yellowfish Labeobarbus marequensis Smith 1841 (Teleostei: Cypriniformes: Cyprinidae). J. Morphol., 281, 997-1009. DOI: 10.1002/jmor.21228
Żelazowska, M., & Kujawa, R. (2022). Microscopic study of the primary growth ovarian follicles of the pike-perch Sander lucioperca (Linnaeus 1758) (Actinopterygii, Perciformes). Micron, 160, 103318. DOI: 10.1016/j.micron.2022.103318
Zlotina, A., Dedukh, D., & Krasikova, A. (2017). Amphibian and avian karyotype evolution: insights from lampbrush chromosome studies. Genes, 8, 311. DOI: 10.3390/genes8110311

Ayrıntılar

Birincil Dil

İngilizce

Konular

Genetik (Diğer)

Bölüm

Derleme

Yazarlar

Nadim Yılmazer ^*
0000-0002-9935-9608
Türkiye

Melek Keskin Başpınar Bu kişi benim
0000-0003-0805-337X
Türkiye

Erken Görünüm Tarihi

18 Temmuz 2025

Yayımlanma Tarihi

31 Temmuz 2025

Gönderilme Tarihi

8 Nisan 2025

Kabul Tarihi

3 Temmuz 2025

Yayımlandığı Sayı

Yıl 2025 Cilt: 10 Sayı: 4

DOI

https://doi.org/10.35229/jaes.1667709

IZ

https://izlik.org/JA54AA53RG

APA

Yılmazer, N., & Keskin Başpınar, M. (2025). The First and Current Checklist of the Animal Species Bearing Lampbrush Chromosomes. Journal of Anatolian Environmental and Animal Sciences, 10(4), 431-442. https://doi.org/10.35229/jaes.1667709

JAES, 2016- 11.yıl

İlk ve Güncel Lamba Fırçası Kromozomları Taşıyan Hayvan Türleri Listesi

Öz

Anahtar Kelimeler

The First and Current Checklist of the Animal Species Bearing Lampbrush Chromosomes

Abstract

Keywords

Kaynakça

Ayrıntılar

Birincil Dil

Konular

Bölüm

Yazarlar

Erken Görünüm Tarihi

Yayımlanma Tarihi

Gönderilme Tarihi

Kabul Tarihi

Yayımlandığı Sayı

DOI

IZ

Kaynak Göster