» Articles » PMID: 28306086

Terminal Filament Cell Organization in the Larval Ovary of Drosophila Melanogaster: Ultrastructural Observations and Pattern of Divisions

Overview
Specialty Biology
Date 2017 Mar 18
PMID 28306086
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

The adult ovary of Drosophila is composed of approximately twenty parallel repetitive structures called ovarioles. The ovarioles appear at the prepupal stage and their formation requires the presence of stacks of discshaped cells called the terminal filaments. Terminal filaments form in a progressive manner during the third larval instar. We have looked at the beginning of formation of both the terminal filaments and ovarioles at an ultrastructural level. Moreover, we studied the pattern of division of the terminal filament cell precursors using the base analog, BrdU. Two main waves of division are observed. The first wave consists of divisions of almost all the terminal filament cell precursors during a short period of time at the transition between the second and third larval instar. The second wave, in which the precursors carry out their final divisions before differentiating, occurs gradually, going from the medial to the lateral side of the ovary during the first half of the third larval instar.

Citing Articles

Gene Protein Sequence Evolution Can Predict the Rapid Divergence of Ovariole Numbers in the Drosophila melanogaster Subgroup.

Whittle C, Extavour C Genome Biol Evol. 2024; 16(7).

PMID: 38848313 PMC: 11272079. DOI: 10.1093/gbe/evae118.


Catalytic activity of the Bin3/MePCE methyltransferase domain is dispensable for 7SK snRNP function in Drosophila melanogaster.

Palumbo R, Yang Y, Feigon J, Hanes S Genetics. 2023; 226(1).

PMID: 37982586 PMC: 10763541. DOI: 10.1093/genetics/iyad203.


Distinct gene expression dynamics in germ line and somatic tissue during ovariole morphogenesis in Drosophila melanogaster.

Tarikere S, Ylla G, Extavour C G3 (Bethesda). 2021; 12(2).

PMID: 34849771 PMC: 9210308. DOI: 10.1093/g3journal/jkab305.


Adult stem cells and niche cells segregate gradually from common precursors that build the adult ovary during pupal development.

Reilein A, Kogan H, Misner R, Park K, Kalderon D Elife. 2021; 10.

PMID: 34590579 PMC: 8536258. DOI: 10.7554/eLife.69749.


A transitory signaling center controls timing of primordial germ cell differentiation.

Banisch T, Slaidina M, Gupta S, Ho M, Gilboa L, Lehmann R Dev Cell. 2021; 56(12):1742-1755.e4.

PMID: 34081907 PMC: 8330407. DOI: 10.1016/j.devcel.2021.05.008.


References
1.
Maine E, Kimble J . Genetic control of cell communication in C. elegans development. Bioessays. 1990; 12(6):265-71. DOI: 10.1002/bies.950120604. View

2.
Sahut-Barnola I, Godt D, Laski F, Couderc J . Drosophila ovary morphogenesis: analysis of terminal filament formation and identification of a gene required for this process. Dev Biol. 1995; 170(1):127-35. DOI: 10.1006/dbio.1995.1201. View

3.
Reynolds E . The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963; 17:208-12. PMC: 2106263. DOI: 10.1083/jcb.17.1.208. View

4.
King R, Aggarwal S, Aggarwal U . The development of the female Drosophila reproductive system. J Morphol. 1968; 124(2):143-66. DOI: 10.1002/jmor.1051240203. View

5.
Godt D, Laski F . Mechanisms of cell rearrangement and cell recruitment in Drosophila ovary morphogenesis and the requirement of bric à brac. Development. 1995; 121(1):173-87. DOI: 10.1242/dev.121.1.173. View