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Journal articles on the topic 'Gonadogenesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 April 2022

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1

Dufourcq, Pascale, Martin Victor, Frédérique Gay, Dominica Calvo, Jonathan Hodgkin, and Yang Shi. "Functional Requirement for Histone Deacetylase 1 in Caenorhabditis elegans Gonadogenesis." Molecular and Cellular Biology 22, no. 9 (2002): 3024–34. http://dx.doi.org/10.1128/mcb.22.9.3024-3034.2002.

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ABSTRACT Histone acetylation and deacetylation have been implicated in the regulation of gene expression. Molecular studies have shown that histone deacetylases (HDACs) function as transcriptional repressors. However, very little is known about their roles during development in multicellular organisms. We previously demonstrated that inhibition of maternal and zygotic expression of histone deacetylase 1 (HDA-1) causes embryonic lethality in Caenorhabditis elegans. Here, we report the identification of an hda-1 genetic mutant which has also been called a gon-10 mutant (for gonadogenesis defecti

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2

Piferrer, Francesc. "Epigenetics of sex determination and gonadogenesis." Developmental Dynamics 242, no. 4 (2013): 360–70. http://dx.doi.org/10.1002/dvdy.23924.

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3

Civinini, Annalena, Stefania Petrucci, and ValentinaP Gallo. "Chick gonadogenesis following early surgical bursectomy." Anatomy and Embryology 187, no. 6 (1993): 557–64. http://dx.doi.org/10.1007/bf00214434.

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4

Smith, Craig A., and Jean M. P. Joss. "Sertoli cell differentiation and gonadogenesis inAlligator mississippiensis." Journal of Experimental Zoology 270, no. 1 (1994): 57–70. http://dx.doi.org/10.1002/jez.1402700107.

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5

Hliwa, Piotr, Andrzej Żyła, and Jarosław Król. "Gonadogenesis in Chub Squalius (Leuciscus) cephalus (L. 1758)." Folia Biologica 57, no. 3 (2009): 115–20. http://dx.doi.org/10.3409/fb57_3-4.115-120.

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6

Smith, Craig A., Matthijs J. Smith, and Andrew H. Sinclair. "Gene expression during gonadogenesis in the chicken embryo." Gene 234, no. 2 (1999): 395–402. http://dx.doi.org/10.1016/s0378-1119(99)00179-1.

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7

Yaba, Aylin, N. Ece Gungor Ordueri, Gamze Tanriover, Pinar Sahin, Necdet Demir, and Ciler Celik-Ozenci. "Expression of CCM2 and CCM3 during mouse gonadogenesis." Journal of Assisted Reproduction and Genetics 32, no. 10 (2015): 1497–507. http://dx.doi.org/10.1007/s10815-015-0559-2.

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8

Intarapat, Sittipon, and Orawan Satayalai. "Microanatomical Study of Embryonic Gonadal Development in Japanese Quail (Coturnix japonica)." Anatomy Research International 2014 (September 3, 2014): 1–9. http://dx.doi.org/10.1155/2014/168614.

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Gonadal development of quail embryos was examined histologically using histological and histochemical methods. In the present study, quail embryos were studied at various stages of incubation period based on phases of gonadogenesis. Germ cell migration was observed on day 3-4 but gonadal differentiation and gonadal function were observed on day 6–8 and day 11–14, respectively. During germ cell migration, quail primordial germ cells (qPGCs) were successfully detected in both left and right genital ridges as well as the dorsal mesentery by lectin histochemistry. Unexpectedly, qPGCs-like cells we

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9

Choi, Hee-Jung, Sung-Young Oh, Jung-Goo Myoung, et al. "Sex Differentiation and Early Gonadogenesis in Sebastes inermis Cuvier." Ocean and Polar Research 30, no. 4 (2008): 401–6. http://dx.doi.org/10.4217/opr.2008.30.4.401.

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10

Vernet, Guy, and Jacques Bierne. "Neuroendocrine control of gonadogenesis in regenerating Lineus lacteus (Heteronemertea)." Hydrobiologia 156, no. 1 (1988): 53–60. http://dx.doi.org/10.1007/bf00027978.

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11

Hardisty, M. W. "Sex differentiation and gonadogenesis in lampreys (Part I and II)." Proceedings of the Zoological Society of London 146, no. 3 (2010): 305–45. http://dx.doi.org/10.1111/j.1469-7998.1965.tb05214.x.

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12

Hardisty, M. W. "Sex differentiation and gonadogenesis in lampreys (Parts I and II)." Proceedings of the Zoological Society of London 146, no. 3 (2010): 346–87. http://dx.doi.org/10.1111/j.1469-7998.1965.tb05215.x.

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13

Mathies, L. D. "The C. elegans Hand gene controls embryogenesis and early gonadogenesis." Development 130, no. 13 (2003): 2881–92. http://dx.doi.org/10.1242/dev.00483.

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14

Lin, Li-Hsien, and Robert M. DePhilip. "Sex-dependent expression of placental (P)-cadherin during mouse gonadogenesis." Anatomical Record 246, no. 4 (1996): 535–44. http://dx.doi.org/10.1002/(sici)1097-0185(199612)246:4<535::aid-ar12>3.0.co;2-p.

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15

Hardisty, M. W., I. C. Potter, and J. D. Koehn. "Gonadogenesis and sex differentiation in the southern hemisphere lampreyMordacia mordax." Journal of Zoology 226, no. 3 (1992): 491–516. http://dx.doi.org/10.1111/j.1469-7998.1992.tb07494.x.

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16

Ebrahimzadeh Bideskan, Alireza, F. Nikmard, M. Sankian, and A. R. Fazel. "Laminin B1 expression during gonadogenesis in rat using immunohistochemical technique." Clinical Biochemistry 44, no. 13 (2011): S11—S12. http://dx.doi.org/10.1016/j.clinbiochem.2011.08.035.

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17

Zhao, Chunyan, Shihong Xu, Yifan Liu, Yanfeng Wang, Qinghua Liu, and Jun Li. "Gonadogenesis analysis and sex differentiation in cultured turbot (Scophthalmus maximus)." Fish Physiology and Biochemistry 43, no. 1 (2016): 265–78. http://dx.doi.org/10.1007/s10695-016-0284-5.

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18

Sun, Andrew Y., and Eric J. Lambie. "gon-2, a Gene Required for Gonadogenesis in Caenorhabditis elegans." Genetics 147, no. 3 (1997): 1077–89. http://dx.doi.org/10.1093/genetics/147.3.1077.

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The gonad of the Caenorhabditis elegans hermaphrodite is generated by the postembryonic divisions of two somatic precursors, Z1 and Z4, and two germline precursors, Z2 and Z3. These cells begin division midway through the first larval stage. By the end of the fourth larval stage, Z1 and Z4 produce 143 descendants, while Z2 and Z3 give rise to ∼1000 descendants. The divisions of Z2 and Z3 are dependent on signals produced by Z1 and Z4, but not vice versa. We have characterized the properties of five loss-of-function alleles of a newly described gene, which we call gon-2. In gon-2 mutants, gonad

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19

Siegfried, Kellee R., and Judith Kimble. "POP-1 controls axis formation during early gonadogenesis inC. elegans." Development 129, no. 2 (2002): 443–53. http://dx.doi.org/10.1242/dev.129.2.443.

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The shape and polarity of the C. elegans gonad is defined during early gonadogenesis by two somatic gonadal precursor cells, Z1 and Z4, and their descendants. Z1 and Z4 divide asymmetrically to establish the proximal-distal axes of the gonad and to generate regulatory leader cells that control organ shape. In this paper, we report that pop-1, the C. elegans TCF/LEF-1 transcription factor, controls the first Z1/Z4 asymmetric division and hence controls proximal-distal axis formation. We have identified two pop-1(Sys) alleles (for symmetrical sisters) that render the Z1/Z4 divisions symmetrical.

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20

Piprek, Rafał P., Anna Pecio, Jacek Z. Kubiak та Jacek M. Szymura. "Differential effects of testosterone and 17β-estradiol on gonadal development in five anuran species". REPRODUCTION 144, № 2 (2012): 257–67. http://dx.doi.org/10.1530/rep-12-0048.

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Sex hormones are essential for sexual differentiation and play a key role in the development of gonads in amphibians. The goal of this study was to evaluate the influence of exogenous sex steroids, testosterone, and 17β-estradiol (E2) on development of gonads in five anuran species differing in their evolutionary positions, sex determination, and mode of gonadogenesis. We found that in two closely related species of fire-bellied toad, Bombina bombina and Bombina variegata, testosterone and E2 exposure results in sex reversal as well as intersex and undifferentiated gonads. Similarly, sex rever

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21

Parmentier, H. K., and L. P. M. Timmermans. "The differentiation of germ cells and gonads during development of carp (Cyprinus carpio L.). A study with anti-carp sperm monoclonal antibodies." Development 90, no. 1 (1985): 13–32. http://dx.doi.org/10.1242/dev.90.1.13.

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Gonadal development, germ cell differentiation and the appearance of membrane antigenic determinants, specific for male and female germ cells during gonadogenesis, was studied in larval and juvenile carp (Cyprinus carpio L.) until 25 weeks after fertilization Indirect immunofluorescence studies with four monoclonal antibodies raised against carp spermatozoa revealed that monoclonal antibody WCS 29 stained the outer membranes of primordial germ cells in larvae from 3 days after fertilization. The monoclonal antibodies WCS 3 and 17 reacted with the outer membranes of germ cells from 7 weeks afte

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22

Migaud, H., R. Mandiki, J. N. Gardeur, P. Kestemont, N. Bromage, and P. Fontaine. "Influence of photoperiod regimes on the Eurasian perch gonadogenesis and spawning." Fish Physiology and Biochemistry 28, no. 1-4 (2003): 395–97. http://dx.doi.org/10.1023/b:fish.0000030604.04618.d7.

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23

Goo, In Bon, Jung Eun Kim, Myung Hun Kim, et al. "Gonadogenesis and Sex Differentiation in the Korean Rose Bitterling, Rhodeus uyekii)." Development & Reproduction 20, no. 4 (2016): 289–96. http://dx.doi.org/10.12717/dr.2016.20.4.289.

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24

Penman, David J., and Francesc Piferrer. "Fish Gonadogenesis. Part I: Genetic and Environmental Mechanisms of Sex Determination." Reviews in Fisheries Science 16, sup1 (2008): 16–34. http://dx.doi.org/10.1080/10641260802324610.

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25

Piferrer, Francesc, and Yann Guiguen. "Fish Gonadogenesis. Part II: Molecular Biology and Genomics of Sex Differentiation." Reviews in Fisheries Science 16, sup1 (2008): 35–55. http://dx.doi.org/10.1080/10641260802324644.

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26

Harikae, Kyoko, Kento Miura, and Yoshiakira Kanai. "Early gonadogenesis in mammals: Significance of long and narrow gonadal structure." Developmental Dynamics 242, no. 4 (2012): 330–38. http://dx.doi.org/10.1002/dvdy.23872.

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27

Lin, Yi-Tzu, Lindsey Barske, Tony DeFalco, and Blanche Capel. "Numb regulates somatic cell lineage commitment during early gonadogenesis in mice." Development 144, no. 9 (2017): 1607–18. http://dx.doi.org/10.1242/dev.149203.

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28

Ziel, Joshua W., David Q. Matus, and David R. Sherwood. "An expression screen for RhoGEF genes involved in C. elegans gonadogenesis." Gene Expression Patterns 9, no. 6 (2009): 397–403. http://dx.doi.org/10.1016/j.gep.2009.06.005.

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29

Voutev, Roumen, Darrell J. Killian, James Hyungsoo Ahn, and E. Jane Albert Hubbard. "Alterations in ribosome biogenesis cause specific defects in C. elegans hermaphrodite gonadogenesis." Developmental Biology 298, no. 1 (2006): 45–58. http://dx.doi.org/10.1016/j.ydbio.2006.06.011.

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30

Flament, S., S. Kuntz, A. Chesnel, et al. "Effect of cadmium on gonadogenesis and metamorphosis in Pleurodeles waltl (urodele amphibian)." Aquatic Toxicology 64, no. 2 (2003): 143–53. http://dx.doi.org/10.1016/s0166-445x(03)00042-0.

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31

Chesney, Michael A., Ngan Lam, Dyan E. Morgan, Bryan T. Phillips, and Judith Kimble. "C. elegans HLH-2/E/Daughterless controls key regulatory cells during gonadogenesis." Developmental Biology 331, no. 1 (2009): 14–25. http://dx.doi.org/10.1016/j.ydbio.2009.04.015.

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32

Kalinina, M. V., N. A. Vinnikova, and E. G. Semen’kova. "Gonadogenesis and color characteristics of ovaries in Japanese mitten crab Eriocheir japonicus." Russian Journal of Developmental Biology 39, no. 1 (2008): 52–58. http://dx.doi.org/10.1134/s1062360408010086.

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33

Hardisty, M. W., I. C. Potter, and R. W. Hilliard. "Gonadogenesis and sex differentiation in the southern hemisphere lamprey, Geotria australis Gray." Journal of Zoology 209, no. 4 (1986): 477–99. http://dx.doi.org/10.1111/j.1469-7998.1986.tb03606.x.

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34

Cui, S. "Disrupted gonadogenesis and male-to-female sex reversal in Pod1 knockout mice." Development 131, no. 16 (2004): 4095–105. http://dx.doi.org/10.1242/dev.01266.

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35

El Jamil, Anwar, Rasha Kanhoush, Solange Magre, Brigitte Boizet-Bonhoure, and May Penrad-Mobayed. "Sex-specific expression of SOX9 during gonadogenesis in the amphibian Xenopus tropicalis." Developmental Dynamics 237, no. 10 (2008): 2996–3005. http://dx.doi.org/10.1002/dvdy.21692.

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36

Friedman, Lisa, Sonia Santa Anna-Arriola, Jonathan Hodgkin, and Judith Kimble. "gon-4, a Cell Lineage Regulator Required for Gonadogenesis in Caenorhabditis elegans." Developmental Biology 228, no. 2 (2000): 350–62. http://dx.doi.org/10.1006/dbio.2000.9944.

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37

Miskowski, Jennifer, Yongjing Li, and Judith Kimble. "The sys-1 Gene and Sexual Dimorphism during Gonadogenesis in Caenorhabditis elegans." Developmental Biology 230, no. 1 (2001): 61–73. http://dx.doi.org/10.1006/dbio.2000.9998.

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38

Sarraj, Mai A., Mai A. Sarraj, Hui Kheng Chua, et al. "Differential expression of TGFBR3 (betaglycan) in mouse ovary and testis during gonadogenesis." Growth Factors 25, no. 5 (2007): 334–45. http://dx.doi.org/10.1080/08977190701833619.

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39

Smith, CA, V. Clifford, PS Western, SA Wilcox, KS Bell, and AH Sinclair. "Cloning and expression of a DAX1 homologue in the chicken embryo." Journal of Molecular Endocrinology 24, no. 1 (2000): 23–32. http://dx.doi.org/10.1677/jme.0.0240023.

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DAX1 is an unusual member of the orphan nuclear receptor family of transcription factors. Mutations in human DAX1 cause X-linked adrenal hypoplasia congenita, while abnormal duplication of the gene is responsible for male-to-female dosage-sensitive sex reversal. Based on these and other observations, DAX1 is thought to play a role in adrenal and gonadal development in mammals. As DAX1 has not previously been described in any other vertebrate, a putative avian DAX1 clone was isolated from an embryonic chicken (Gallus domesticus) urogenital ridge cDNA library. The expression profile of this cDNA

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40

Boyle, M., N. Bonini, and S. DiNardo. "Expression and function of clift in the development of somatic gonadal precursors within the Drosophila mesoderm." Development 124, no. 5 (1997): 971–82. http://dx.doi.org/10.1242/dev.124.5.971.

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The gonad forms from cells of two lineages: the germline and soma. The somatic gonadal cells generate the various cell types within the testis or ovary that support gametogenesis. These cells derive from embryonic mesoderm, but how they are specified is unknown. Here, we describe a novel regulator of Drosophila gonadogenesis, clift, mutations in which abolish gonad formation. clift is expressed within somatic gonadal precursors as these cells first form, demonstrating that 9–12 cells are selected as somatic gonadal precursors within each of three posterior parasegments at early stages in gonad

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41

Boyle, M., and S. DiNardo. "Specification, migration and assembly of the somatic cells of the Drosophila gonad." Development 121, no. 6 (1995): 1815–25. http://dx.doi.org/10.1242/dev.121.6.1815.

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The adult ovaries and testes contain several specialized somatic cell types that support the differentiation of germ cells into mature gametes. Each of these cell types arise from mesodermal cells that constitute the embryonic gonad. To explore the mechanisms governing the development and differentiation of these cells, we focus on the formation of the gonad during Drosophila development. Using markers for the precursors of the somatic cells of the gonad, we identify discrete steps in the development of the gonad. Our results suggest the existence of different populations of gonadal precursors

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42

Estermann, Martin A., and Craig A. Smith. "Applying Single-Cell Analysis to Gonadogenesis and DSDs (Disorders/Differences of Sex Development)." International Journal of Molecular Sciences 21, no. 18 (2020): 6614. http://dx.doi.org/10.3390/ijms21186614.

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The gonads are unique among the body’s organs in having a developmental choice: testis or ovary formation. Gonadal sex differentiation involves common progenitor cells that form either Sertoli and Leydig cells in the testis or granulosa and thecal cells in the ovary. Single-cell analysis is now shedding new light on how these cell lineages are specified and how they interact with the germline. Such studies are also providing new information on gonadal maturation, ageing and the somatic-germ cell niche. Furthermore, they have the potential to improve our understanding and diagnosis of Disorders

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43

Karp, Xantha, and Iva Greenwald. "Multiple roles for the E/Daughterless ortholog HLH-2 during C. elegans gonadogenesis." Developmental Biology 272, no. 2 (2004): 460–69. http://dx.doi.org/10.1016/j.ydbio.2004.05.015.

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44

Migaud, Hervé, Pascal Fontaine, Patrick Kestemont, Neil Wang, and Jean Brun-Bellut. "Influence of photoperiod on the onset of gonadogenesis in Eurasian perch Perca fluviatilis." Aquaculture 241, no. 1-4 (2004): 561–74. http://dx.doi.org/10.1016/j.aquaculture.2004.07.031.

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45

Matrosova, Inga V., and Vladimir V. Evdokimov. "Seasonal characteristic of gonadogenesis for the sea cucumber Apostichopus japonicus Selenka." Izvestiya TINRO 185, no. 2 (2016): 112–22. http://dx.doi.org/10.26428/1606-9919-2016-185-112-122.

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Gonads of females and males of the sea cucumber Apostichopus japonicus were collected along Primorye coast of the Japan Sea (bays Kiyevka, Sokolovskaya, Melkovodnaya, Sredniaya, and the area between Cape Genbachev and Cape DeLivron) in different seasons from May to October, 2011. The gonads were fixed in 70 % alcohol and Buena fixing agent, using Isoprep and Histomix, and subjected to histophyisiological analysis. Sex of the animals and condition of their gonads were defined visually and on histological preparations. Their whole bodies, skin and muscular bags, and sexual glands were weighted,

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46

Liu, Bowen, Shangfeng Liu, Shan He, Ying Zhao, Hongxia Hu, and Zhao Wang. "Cloning and Expression Analysis of Gonadogenesis-associated Gene SPATA4 from Rainbow Trout (Oncorhynchus mykiss)." BMB Reports 38, no. 2 (2005): 206–10. http://dx.doi.org/10.5483/bmbrep.2005.38.2.206.

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47

Yousefian, M. "Sex differentiation by gonadogenesis and sex steroid hormones in cultured great sturgeon (Huso huso)." Journal of Applied Ichthyology 22, s1 (2006): 369–72. http://dx.doi.org/10.1111/j.1439-0426.2007.00987.x.

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48

Qin, Mingming, Zhiwei Zhang, Weiyi Song, et al. "Roles of Figla/figla in Juvenile Ovary Development and Follicle Formation During Zebrafish Gonadogenesis." Endocrinology 159, no. 11 (2018): 3699–722. http://dx.doi.org/10.1210/en.2018-00648.

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49

Liu, Xiao-Ling, Yun Li, Jian-Guo Liu, Long-Bo Cui, and Zhi-Feng Zhang. "Gonadogenesis in scallop Chlamys farreri and Cf-foxl2 expression pattern during gonadal sex differentiation." Aquaculture Research 47, no. 5 (2014): 1605–11. http://dx.doi.org/10.1111/are.12621.

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50

Stoop, H., F. Honecker, M. Cools, R. de Krijger, C. Bokemeyer, and L. H. J. Looijenga. "Differentiation and development of human female germ cells during prenatal gonadogenesis: an immunohistochemical study." Human Reproduction 20, no. 6 (2005): 1466–76. http://dx.doi.org/10.1093/humrep/deh800.

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