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How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies

Under conditions in which budding yeast form colonies and then undergo meiosis/sporulation, the resulting colonies are organized such that a sharply defined layer of meiotic cells overlays a layer of unsporulated cells termed “feeder cells.” This differentiation pattern requires activation of both t...

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Autores principales: Piccirillo, Sarah, McCune, Abbigail H., Dedert, Samuel R., Kempf, Cassandra G., Jimenez, Brian, Solst, Shane R., Tiede-Lewis, LeAnn M., Honigberg, Saul M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893387/
https://www.ncbi.nlm.nih.gov/pubmed/31619446
http://dx.doi.org/10.1534/genetics.119.302700
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author Piccirillo, Sarah
McCune, Abbigail H.
Dedert, Samuel R.
Kempf, Cassandra G.
Jimenez, Brian
Solst, Shane R.
Tiede-Lewis, LeAnn M.
Honigberg, Saul M.
author_facet Piccirillo, Sarah
McCune, Abbigail H.
Dedert, Samuel R.
Kempf, Cassandra G.
Jimenez, Brian
Solst, Shane R.
Tiede-Lewis, LeAnn M.
Honigberg, Saul M.
author_sort Piccirillo, Sarah
collection PubMed
description Under conditions in which budding yeast form colonies and then undergo meiosis/sporulation, the resulting colonies are organized such that a sharply defined layer of meiotic cells overlays a layer of unsporulated cells termed “feeder cells.” This differentiation pattern requires activation of both the Rlm1/cell-wall integrity pathway and the Rim101/alkaline-response pathway. In the current study, we analyzed the connection between these two signaling pathways in regulating colony development by determining expression patterns and cell-autonomy relationships. We present evidence that two parallel cell-nonautonomous positive-feedback loops are active in colony patterning, an Rlm1-Slt2 loop active in feeder cells and an Rim101-Ime1 loop active in meiotic cells. The Rlm1-Slt2 loop is expressed first and subsequently activates the Rim101-Ime1 loop through a cell-nonautonomous mechanism. Once activated, each feedback loop activates the cell fate specific to its colony region. At the same time, cell-autonomous mechanisms inhibit ectopic fates within these regions. In addition, once the second loop is active, it represses the first loop through a cell-nonautonomous mechanism. Linked cell-nonautonomous positive-feedback loops, by amplifying small differences in microenvironments, may be a general mechanism for pattern formation in yeast and other organisms.
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spelling pubmed-68933872019-12-05 How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies Piccirillo, Sarah McCune, Abbigail H. Dedert, Samuel R. Kempf, Cassandra G. Jimenez, Brian Solst, Shane R. Tiede-Lewis, LeAnn M. Honigberg, Saul M. Genetics Investigations Under conditions in which budding yeast form colonies and then undergo meiosis/sporulation, the resulting colonies are organized such that a sharply defined layer of meiotic cells overlays a layer of unsporulated cells termed “feeder cells.” This differentiation pattern requires activation of both the Rlm1/cell-wall integrity pathway and the Rim101/alkaline-response pathway. In the current study, we analyzed the connection between these two signaling pathways in regulating colony development by determining expression patterns and cell-autonomy relationships. We present evidence that two parallel cell-nonautonomous positive-feedback loops are active in colony patterning, an Rlm1-Slt2 loop active in feeder cells and an Rim101-Ime1 loop active in meiotic cells. The Rlm1-Slt2 loop is expressed first and subsequently activates the Rim101-Ime1 loop through a cell-nonautonomous mechanism. Once activated, each feedback loop activates the cell fate specific to its colony region. At the same time, cell-autonomous mechanisms inhibit ectopic fates within these regions. In addition, once the second loop is active, it represses the first loop through a cell-nonautonomous mechanism. Linked cell-nonautonomous positive-feedback loops, by amplifying small differences in microenvironments, may be a general mechanism for pattern formation in yeast and other organisms. Genetics Society of America 2019-12 2019-10-16 /pmc/articles/PMC6893387/ /pubmed/31619446 http://dx.doi.org/10.1534/genetics.119.302700 Text en Copyright © 2019 by the Genetics Society of America Available freely online through the author-supported open access option.
spellingShingle Investigations
Piccirillo, Sarah
McCune, Abbigail H.
Dedert, Samuel R.
Kempf, Cassandra G.
Jimenez, Brian
Solst, Shane R.
Tiede-Lewis, LeAnn M.
Honigberg, Saul M.
How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies
title How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies
title_full How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies
title_fullStr How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies
title_full_unstemmed How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies
title_short How Boundaries Form: Linked Nonautonomous Feedback Loops Regulate Pattern Formation in Yeast Colonies
title_sort how boundaries form: linked nonautonomous feedback loops regulate pattern formation in yeast colonies
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893387/
https://www.ncbi.nlm.nih.gov/pubmed/31619446
http://dx.doi.org/10.1534/genetics.119.302700
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