linkedin post 2018-10-05 04:17:26

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BIOFILMS. "Some groups of bacterial cells are functionally organized. In lamentous cyanobacteria such as Calothrix and Trichodesmium, poor conditions induce POD in some cells. Because the lament often breaks up as a result, the function of POD in this system could be filament dispersal in response to unfavorable environmental conditions." (POD = programmed organismal death). View in LinkedIn
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linkedin post 2018-10-05 04:22:50

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DEATH GLUE. "Recent studies have revealed that the regulated death of bacterial cells is important for biofilm development. Following cell death, a sub-population of the dead bacteria lyse and release genomic DNA, which then has an essential role in intercellular adhesion and biofilm stability." https://lnkd.in/dm2ekKx View in LinkedIn
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linkedin post 2018-10-05 04:24:27

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GREY ZONE CREATURES. "In eukaryotes as well, the distinction between unicellular and multicellular is not always completely clear. For example, the social amoeba, Dictyostelium discoidium, is unicellular during part of its life cycle, but upon starvation, cells aggregate and develop into a multicellular motile slug, then fruiting body. Stalk cell death is programmed and is characterized by some classic features of POD." (POD = programmed organismal death). View in LinkedIn
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linkedin post 2018-10-05 04:30:13

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SELFISH MOBILE GENETIC ELEMENTS. "In some cases, this peculiar form of selection may explain the function and evolution of genes for unicell POD. When a cell has low chances for reproduction, POD and the transfer of genes from the dying cell to a new host can save the genes. This process may be associated with occurrence of new mutations in the transferred genes and their improved ability to survive in the new host." (POD = programmed organismal death). View in LinkedIn
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linkedin post 2018-10-05 04:33:23

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PARADOXICAL POISON AND ANTIDOTE. "In prokaryotes, conjugative plasmids often encode for the simultaneous production of long-lived toxins and short-lived antitoxins. When these are present together, the toxin is harmless to the host. However, if one daughter cell is cured of the plasmid, it will inherit toxic cytoplasm without a source of antitoxin and will die. While this is easily explained as a ‘selfish’ adaptation on the part of the plasmid, chromosomally-encoded toxin-antitoxin systems probably do not function in gene-level competition." https://www.linkedin.com/redir/general-malware-page?url=http%3A%2F%2Fwww%2eesciencecentral%2eorg%2Fjournals%2Fare-internal-death-promoting-mechanisms-ever-adaptive-2329-9002%2e1000113%2epdf View in LinkedIn
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linkedin post 2018-10-05 04:36:36

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GENE OWNERSHIP. "Plasmids and bacteriophages may induce cell death in the host (or non-host daughter) cell. Whether or not this is considered an example of programmed organismal death, of course, hinges on whether or not selfish genetic elements are considered part of the organismal genome. The benefits in this case are straightforward and focused on the level of the selfish genetic element." View in LinkedIn
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linkedin post 2018-10-06 03:57:25

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FRAGMENT FROM NATURE concludes this weekend on the Wolbachia theme which reveals unusual gene transfers during parasitism. Parasitism has long been likened to an arms race, although like everything else in Nature, there is a broad Bell curve. Between the Wolbachia bacteria, the bacteriophage WO virus that preys on the Wolbachia bacteria, and the eukaryotic host, there is shown to be liberal gene exchange, enriching the adaptive toolbox. More than likely, this is far from an isolated case. https://lnkd.in/dZe2vg8 View in LinkedIn
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linkedin post 2018-10-06 04:01:46

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ABUNDANT GENE MECHANISMS IN PHAGES. "WO is a dynamic element that has a significant impact on the genetic diversity of Wolbachia. Analysis shows that WO molecular evolution is a complex process involving vertical transmission and horizontal transfer, recombination between phages, and hitchhiking of other mobile elements on WO." https://lnkd.in/dG3vir9 View in LinkedIn
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linkedin post 2018-10-06 04:03:54

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ADDING A SECOND DOMAIN. "Here we assemble the sequenced genomes of phage WO particles, resolve the bacteriophage attachment and bacterial integration sites, report a eukaryotic association module in bacteriophages and discuss lateral gene transfers between eukaryotes and bacteriophages." https://lnkd.in/dYh3-r4 View in LinkedIn
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