Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids

Metakaryotic cells and syncytia with large, hollow, bell-shaped nuclei demonstrate symmetrical and asymmetrical amitotic nuclear fissions in microanatomical positions and numbers expected of stem cell lineages in tissues of all three primordial germ layers and their derived tumors. Using fluorescenc...

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Main Authors: Gostjeva, Elena V., Fomina, Janna N., Darroudi, Firouz, Gruhl, Amanda Natalie, Thilly, William G
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: Elsevier 2015
Online Access:http://hdl.handle.net/1721.1/99524
https://orcid.org/0000-0002-4232-261X
https://orcid.org/0000-0003-2581-6092
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author Gostjeva, Elena V.
Fomina, Janna N.
Darroudi, Firouz
Gruhl, Amanda Natalie
Thilly, William G
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Gostjeva, Elena V.
Fomina, Janna N.
Darroudi, Firouz
Gruhl, Amanda Natalie
Thilly, William G
author_sort Gostjeva, Elena V.
collection MIT
description Metakaryotic cells and syncytia with large, hollow, bell-shaped nuclei demonstrate symmetrical and asymmetrical amitotic nuclear fissions in microanatomical positions and numbers expected of stem cell lineages in tissues of all three primordial germ layers and their derived tumors. Using fluorescence in situ hybridization, mononuclear metakaryotic interphase cells have been found with only 23 centromeric and 23 telomeric staining regions. Syncytial bell-shaped nuclei found approximately during weeks 5–12 of human gestation display 23 centromeric and either 23 or 46 telomeric staining regions. These images suggest that (1) homologous chromatids pair at centromeres and telomeres, (2) all paired telomeres join end-to-end with other paired telomeres in all mononuclear and some syncytial metakaryotic cells, and (3) telomere junctions may open and close during the syncytial phase of development. Twenty-three telomeric joining figures could be accounted by 23 rings of one chromatid pair each, a single pangenomic ring of 23 joined chromatid pairs, or any of many possible sets of oligo-chromatid pair rings. As telomeric end-joining may affect peri-telomeric gene expression, a programmed sequence of telomeric end-joining associations in metakaryotic stem cells could guide developmental arboration and errors in, or interruptions of, this program could contribute to carcinogenesis.
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spelling mit-1721.1/995242022-09-27T21:30:57Z Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids Gostjeva, Elena V. Fomina, Janna N. Darroudi, Firouz Gruhl, Amanda Natalie Thilly, William G Massachusetts Institute of Technology. Department of Biological Engineering MIT Edgerton Center Gruhl, Amanda Natalie Gostjeva, Elena V. Thilly, William G. Metakaryotic cells and syncytia with large, hollow, bell-shaped nuclei demonstrate symmetrical and asymmetrical amitotic nuclear fissions in microanatomical positions and numbers expected of stem cell lineages in tissues of all three primordial germ layers and their derived tumors. Using fluorescence in situ hybridization, mononuclear metakaryotic interphase cells have been found with only 23 centromeric and 23 telomeric staining regions. Syncytial bell-shaped nuclei found approximately during weeks 5–12 of human gestation display 23 centromeric and either 23 or 46 telomeric staining regions. These images suggest that (1) homologous chromatids pair at centromeres and telomeres, (2) all paired telomeres join end-to-end with other paired telomeres in all mononuclear and some syncytial metakaryotic cells, and (3) telomere junctions may open and close during the syncytial phase of development. Twenty-three telomeric joining figures could be accounted by 23 rings of one chromatid pair each, a single pangenomic ring of 23 joined chromatid pairs, or any of many possible sets of oligo-chromatid pair rings. As telomeric end-joining may affect peri-telomeric gene expression, a programmed sequence of telomeric end-joining associations in metakaryotic stem cells could guide developmental arboration and errors in, or interruptions of, this program could contribute to carcinogenesis. National Institute of Environmental Health Sciences United Therapeutics, Inc. 2015-10-30T15:21:04Z 2015-10-30T15:21:04Z 2010-12 2010-08 Article http://purl.org/eprint/type/JournalArticle 01654608 http://hdl.handle.net/1721.1/99524 Gruhl, Amanda N., Elena V. Gostjeva, William G. Thilly, Janna N. Fomina, and Firouz Darroudi. “Human Fetal/tumor Metakaryotic Stem Cells: Pangenomic Homologous Pairing and Telomeric End-Joining of Chromatids.” Cancer Genetics and Cytogenetics 203, no. 2 (December 2010): 203–208. https://orcid.org/0000-0002-4232-261X https://orcid.org/0000-0003-2581-6092 en_US http://dx.doi.org/10.1016/j.cancergencyto.2010.08.015 Cancer Genetics and Cytogenetics Creative Commons Attribution http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Elsevier PMC
spellingShingle Gostjeva, Elena V.
Fomina, Janna N.
Darroudi, Firouz
Gruhl, Amanda Natalie
Thilly, William G
Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids
title Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids
title_full Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids
title_fullStr Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids
title_full_unstemmed Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids
title_short Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids
title_sort human fetal tumor metakaryotic stem cells pangenomic homologous pairing and telomeric end joining of chromatids
url http://hdl.handle.net/1721.1/99524
https://orcid.org/0000-0002-4232-261X
https://orcid.org/0000-0003-2581-6092
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