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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2019
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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. |
format | Online Article Text |
id | pubmed-6893387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
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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