Karyotype analysis of Meloidogyne hapla by 3-D reconstruction of synaptonemal complexes from electron microscopy of serial sections

Chromosoma ◽  
1978 ◽  
Vol 70 (1) ◽  
pp. 131-139 ◽  
Author(s):  
Paul Goldstein ◽  
A. C. Triantaphyllou
1979 ◽  
Vol 40 (1) ◽  
pp. 171-179
Author(s):  
P. Goldstein ◽  
A.C. Triantaphyllou

Heterodera glycines is a diploid amphimictic nematode with n = 9 chromosomes. Nine normal synaptonemal complexes (SC) were detected following 3-dimensional reconstruction of pachytene nuclei from electron microscopy of serial sections. Regions of unique ‘modified synaptonemal complexes’ (MSC) were observed along 2 SCs. These consist of a heterochromatic knob within which the SC appears either disorganized or stacked in layers of lateral elements. Its function is not known. Recombination nodules and ‘cylindrical granular complexes’, were not observed in H. glycines.


Reproduction ◽  
2012 ◽  
Vol 144 (3) ◽  
pp. 385-392 ◽  
Author(s):  
Unai Silván ◽  
Juan Aréchaga

Cell transplantation into the seminiferous tubules is a useful technique for the study of physiological and pathological conditions affecting the testis. However, the precise three-dimensional organization and, particularly, the complex connectivity of the seminiferous network have not yet been thoroughly characterized. To date, the technical approaches to address these issues have included manual dissection under the stereomicroscope, reconstruction of histological serial sections, and injection of contrast dyes, but all of them have yielded only partial information. Here, using an approach based on the microinjection of a self-polymerizing resin followed by chemical digestion of the surrounding soft tissues, we reveal fine details of the seminiferous tubule scaffold and its connections. These replicas of the testis seminiferous network were studied by scanning electron microscopy. The present results not only establish a morphological basis for more precise microinjection into the mouse seminiferous tubules but also enable a more profound investigation of physiological and embryological features of the testis.


1992 ◽  
Vol 70 (6) ◽  
pp. 1228-1233 ◽  
Author(s):  
James P. Braselton

Sporogenic (cystogenous) stages of development of Spongospora subterranea (Wallroth) Lagerheim f.sp. subterranea Tomlinson infecting potato tubers were examined with transmission electron microscopy. Volume of nuclei in transitional Plasmodia was 28.2 ± 8.3 μm3. Serial section analysis revealed 37 synaptonemal complexes, hence the haploid chromosome number was considered to be 37. Total length of synaptonemal complexes per nucleus was 74.6 ± 1.4 μm, with individual synaptonemal complexes ranging in length from 1.34 ± 0.07 μm to 3.48 ± 0.17 μm. No polycomplexes were observed in transitional nuclei. Electron-opaque thickenings of lateral elements occurred irregularly. Additional ultrastructural features of sporogenic plasmodia included end-to-end paired centrioles defining the poles of the nuclei and a host–parasite boundary of a single unit membrane. Key words: karyotype, Plasmodiophoromycetes, Spongospora, synaptonemal complex.


1980 ◽  
Vol 2 (1-3) ◽  
pp. 265-293 ◽  
Author(s):  
John K. Stevens ◽  
Thomas L. Davis ◽  
Neil Friedman ◽  
Peter Sterling

2021 ◽  
Author(s):  
Linnaea E Ostroff ◽  
Janeth Perez-Garza ◽  
Emily Parrish ◽  
Zachary Deane

Electron microscopy (EM) volume reconstruction is a powerful tool for investigating the fundamental structure of brain circuits, but the full potential of this technique is limited by the difficulty of integrating molecular information. High quality ultrastructural preservation is necessary for EM reconstruction, and intact, highly contrasted cell membranes are essential for following small neuronal processes through serial sections. Unfortunately, the antibody labeling methods used to identify most endogenous molecules result in compromised morphology, especially of membranes. Cryofixation can produce superior morphological preservation and has the additional advantage of allowing indefinite storage of valuable samples. We have developed a method based on cryofixation that allows sensitive immunolabeling of endogenous molecules, preserves excellent ultrastructure, and is compatible with high-contrast staining for serial EM reconstruction.


1984 ◽  
Vol 62 (11) ◽  
pp. 2414-2416 ◽  
Author(s):  
James P. Braselton

Three pachytene nuclei of Polymyxa graminis Ledingham were reconstructed from serial thin sections. Thirty synaptonemal complexes (SCs) were counted, indicating the identical haploid number (30) that was reported for Polymyxa betae. SCs of P. graminis and P. betae were similar in structure, and nuclear volumes and total lengths of SCs per nucleus were not significantly different for the two species.


1976 ◽  
Vol 39 (4) ◽  
pp. 900-908 ◽  
Author(s):  
M. Castel ◽  
M. E. Spira ◽  
I. Parnas ◽  
Y. Yarom

1. The structure of the ventral giant axons of the cockroach at the level of ganglion T3 was studied by means of light and electron microscopy. 2. From serial sections and cobalt injections, the axons diameter was found to range between 40 and 60 mum at the caudal end of ganglion T3; toward the center of T3 they narrow to 20-40 mum, and again expand to 30-45 mum anteriorly in ganglion T3. 3. Each giant axon sends off several branches, 1-15 mum in diameter, into the neuropil. The giant axons and the bases of their branches are enveloped by cytoplasmic processes of glial cells. The periaxonal space is about 100-200 A. 4. Distally the branches are devoid of glial envelopes and the extracellular space between the branches and other axonal profiles is about 200 A. Terminals with presumptive chemical synapses on the giant axon branches were found. Clear vesicles, 300-400 A in diameter, are seen clustered together. The width of the supposedly synaptic gap is about 100 A. 5. In some areas the branches and other axonal profiles form close appositions.


1981 ◽  
Vol 59 (4) ◽  
pp. 419-421 ◽  
Author(s):  
J. Navarro ◽  
F. Vidal ◽  
M. Guitart ◽  
J. Egozcue

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