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Transplantation of Killer Endosymbionts in Paramecium

SEVERAL syngens or breeding groups of Paramecium aurelia contain endosymbionts which may result in the development of the killer trait(1). The symbionts are of different morphological types and it has been suggested that these are non-randomly distributed between syngens(2). Experiments involving cr...

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Detalles Bibliográficos
Autor principal: GIBSON, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 1973
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7095021/
https://www.ncbi.nlm.nih.gov/pubmed/4633042
http://dx.doi.org/10.1038/241127a0
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author GIBSON, I.
author_facet GIBSON, I.
author_sort GIBSON, I.
collection PubMed
description SEVERAL syngens or breeding groups of Paramecium aurelia contain endosymbionts which may result in the development of the killer trait(1). The symbionts are of different morphological types and it has been suggested that these are non-randomly distributed between syngens(2). Experiments involving crosses between paramecia with and without symbionts showed that each endosymbiont required a specific nuclear gene for its maintenance. A single gene controlled the presence or absence of endosymbionts as shown by segregation in the F(2) generation. The pattern of loss of symbionts in some of those F(2) clones varies, generally extending over a number of asexual fissions which for different endosymbionts can be from two to over sixty. Infection experiments also demonstrate the requirement for a specific gene. Infection of endosymbionts from homogenates or purified preparations occurs via the medium but only into particular cells possessing a specific gene(1,3). Finally, some endosymbionts growing in vitro retain their infectivity into certain paramecia (author's laboratory).
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spelling pubmed-70950212020-03-26 Transplantation of Killer Endosymbionts in Paramecium GIBSON, I. Nature Article SEVERAL syngens or breeding groups of Paramecium aurelia contain endosymbionts which may result in the development of the killer trait(1). The symbionts are of different morphological types and it has been suggested that these are non-randomly distributed between syngens(2). Experiments involving crosses between paramecia with and without symbionts showed that each endosymbiont required a specific nuclear gene for its maintenance. A single gene controlled the presence or absence of endosymbionts as shown by segregation in the F(2) generation. The pattern of loss of symbionts in some of those F(2) clones varies, generally extending over a number of asexual fissions which for different endosymbionts can be from two to over sixty. Infection experiments also demonstrate the requirement for a specific gene. Infection of endosymbionts from homogenates or purified preparations occurs via the medium but only into particular cells possessing a specific gene(1,3). Finally, some endosymbionts growing in vitro retain their infectivity into certain paramecia (author's laboratory). Nature Publishing Group UK 1973 /pmc/articles/PMC7095021/ /pubmed/4633042 http://dx.doi.org/10.1038/241127a0 Text en © Nature Publishing Group 1973 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
GIBSON, I.
Transplantation of Killer Endosymbionts in Paramecium
title Transplantation of Killer Endosymbionts in Paramecium
title_full Transplantation of Killer Endosymbionts in Paramecium
title_fullStr Transplantation of Killer Endosymbionts in Paramecium
title_full_unstemmed Transplantation of Killer Endosymbionts in Paramecium
title_short Transplantation of Killer Endosymbionts in Paramecium
title_sort transplantation of killer endosymbionts in paramecium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7095021/
https://www.ncbi.nlm.nih.gov/pubmed/4633042
http://dx.doi.org/10.1038/241127a0
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