<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1405-888X</journal-id>
<journal-title><![CDATA[TIP. Revista especializada en ciencias químico-biológicas]]></journal-title>
<abbrev-journal-title><![CDATA[TIP]]></abbrev-journal-title>
<issn>1405-888X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Facultad de Estudios Superiores Zaragoza]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-888X2024000100009</article-id>
<article-id pub-id-type="doi">10.22201/fesz.23958723e.2024.641</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[El papel del ion calcio y la autofagia en la regulación del hidrotropismo en raíces: el caso de Arabidopsis thaliana]]></article-title>
<article-title xml:lang="en"><![CDATA[The Role of Calcium Ion and Autophagy in Regulating Hydrotropism in Roots: Insights from Arabidopsis thaliana]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Castillo-Olamendi]]></surname>
<given-names><![CDATA[Luis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Jiménez-Nopala]]></surname>
<given-names><![CDATA[Gladys]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Porta]]></surname>
<given-names><![CDATA[Helena]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Nacional Autónoma de México Instituto de Biotecnología Departamento de Biología Molecular de Plantas]]></institution>
<addr-line><![CDATA[Cuernavaca Morelos]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Nacional Autónoma de México Centro de Ciencias Genómicas ]]></institution>
<addr-line><![CDATA[Cuernavaca Morelos]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2024</year>
</pub-date>
<volume>27</volume>
<fpage>0</fpage>
<lpage>0</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-888X2024000100009&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-888X2024000100009&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-888X2024000100009&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Las plantas son organismos sésiles con diferentes mecanismos que intervienen durante la escasez de agua. Uno de ellos es el hidrotropismo que consiste en la modificación del crecimiento y movimiento de la raíz hacia zonas donde hay más agua. Este movimiento es fundamental para la supervivencia de la planta. Otro mecanismo es la autofagia descrita no sólo como una defensa ante la sequía sino también como un proceso catabólico conservado en la mayoría de las células eucariotas, a través del cual se transporta material citoplasmático no deseado o disfuncional a la vacuola de las células vegetales para su degradación y reciclamiento. En la respuesta hidrotrópica, se presenta una acumulación de autofagosomas y H2O2 en la zona de curvatura de la raíz. Por esto la autofagia reduce el estrés oxidativo causado por el estrés hídrico durante el hidrotropismo. El ion calcio (Ca2+) es un segundo mensajero que regula las reacciones al estrés. Cuando la célula percibe un estímulo como la escasez de agua, hay un aumento transitorio o sostenido de la concentración de Ca2+ en el citosol que desencadena procesos celulares temporales al ser detectado por las proteínas fijadoras de Ca2+ como la calmodulina, ubicada en la membrana plasmática y en la membrana de los organelos celulares. La curvatura de la raíz durante el hidrotropismo depende de la acumulación de Ca2+ en el citosol mediante el bloqueo de la ATPasa de Ca2+ ECA1 por la proteína MIZ1. Además, la proteína similar a la calmodulina 24, (CML24), potencialmente se une al Ca2+ en respuesta al estrés abiótico, y al interaccionar con la proteína ATG4 de la autofagia, se puede afectar su progreso. En este trabajo se realizó una revisión de los conceptos básicos del hidrotropismo, la autofagia y el flujo de Ca2+ con la intención de ampliar el conocimiento sobre la interacción de estos procesos y la defensa celular de Arabidopsis thaliana ante la escasez de agua.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Plants are sessile organisms with different mechanisms that intervene during water scarcity. One of them is hydrotropism, which consists of modifying the growth and movement of the root towards areas where there is more water. This movement is essential for the survival of the plant. Another mechanism is autophagy, described not only as a defense against drought but also as a catabolic process conserved in most eukaryotic cells, through which unwanted or dysfunctional cytoplasmic material is transported to the vacuole of plant cells for degradation and recycling. In the hydrotropic response, an accumulation of autophagosomes and H2O2 occurs in the zone of root curvature. For this reason, autophagy reduces oxidative stress caused by water stress during hydrotropism. The calcium ion (Ca2+) is a second messenger that regulates stress reactions. When the cell perceives a stimulus such as water scarcity, there is a transient or sustained increase in the concentration of Ca2+ in the cytosol that triggers temporary cellular processes when detected by Ca2+-binding proteins such as calmodulin, located in the plasma membrane and in the membrane of cellular organelles. Root curvature during hydrotropism depends on Ca2+ accumulation in the cytosol through blockade of the Ca2+ ATPase ECA1 by the MIZ1 protein. Moreover, calmodulin-like protein 24 (CML24) potentially binds Ca2+ in response to abiotic stress, and by interacting with the autophagy protein ATG4, may affect its progress. In this work, a review of the basic concepts of hydrotropism, autophagy and Ca2+ flow was carried out with the intention of expanding knowledge about the interaction of these processes and the cellular defense of Arabidopsis thaliana against water scarcity.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[hidrotropismo]]></kwd>
<kwd lng="es"><![CDATA[autofagia]]></kwd>
<kwd lng="es"><![CDATA[ion calcio]]></kwd>
<kwd lng="es"><![CDATA[escasez de agua]]></kwd>
<kwd lng="en"><![CDATA[hydrotropism]]></kwd>
<kwd lng="en"><![CDATA[autophagy]]></kwd>
<kwd lng="en"><![CDATA[calcium ion]]></kwd>
<kwd lng="en"><![CDATA[water shortage]]></kwd>
</kwd-group>
</article-meta>
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