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1por Sánchez González, José de Jesús, Ruiz Corral, José Ariel, García, Guillermo Medina, Ojeda, Gabriela Ramírez, Larios, Lino De la Cruz, Holland, James Brendan, Medrano, Roberto Miranda, García Romero, Giovanni Emmanuel“…To study the ecogeographic distribution of teosinte we constructed a robust database of 2363 teosinte occurrences from published sources for the period 1842–2016. …”
Publicado 2018
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2por Vann, Laura, Kono, Thomas, Pyhäjärvi, Tanja, Hufford, Matthew B., Ross-Ibarra, Jeffrey“…The teosinte branched1(tb1) gene is a major QTL controlling branching differences between maize and its wild progenitor, teosinte. …”
Publicado 2015
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3“…Here, we used single-nucleotide polymorphism genotyping and data on numerous environmental variables to describe the genetic basis of local adaptation in 21 populations of teosinte, the wild ancestor of maize. We found complex hierarchical genetic structure created by altitude, dispersal events, and admixture among subspecies, which complicated identification of locally beneficial alleles. …”
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4“…RESULTS: To examine how maize evolution and domestication affected meiotic recombination genes, we studied patterns of sequence polymorphism and divergence in eleven genes controlling key steps in the meiotic recombination pathway in a diverse set of maize inbred lines and several accessions of teosinte, the wild ancestor of maize. We discovered that, even though the recombination genes generally exhibited high sequence conservation expected in a pathway controlling a key cellular process, they showed substantial levels and diverse patterns of sequence polymorphism. …”
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5“…One potential line of evidence to explore these relationships is opaline phytoliths produced in teosinte fruit cases. Here we use multidimensional scaling and multiple discriminant analyses to determine if rondel phytolith assemblages from teosinte fruitcases reflect teosinte taxonomy. …”
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6por Trtikova, Miluse, Lohn, Andre, Binimelis, Rosa, Chapela, Ignacio, Oehen, Bernadette, Zemp, Niklaus, Widmer, Alex, Hilbeck, Angelika“…The weed has morphological similarities to a wild relative of maize and has generally been referred to as teosinte. However, the identity, origin or genetic composition of ‘Spanish teosinte’ was unknown. …”
Publicado 2017
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7por Yang, Chin Jian, Samayoa, Luis Fernando, Bradbury, Peter J., Olukolu, Bode A., Xue, Wei, York, Alessandra M., Tuholski, Michael R., Wang, Weidong, Daskalska, Lora L., Neumeyer, Michael A., Sanchez-Gonzalez, Jose de Jesus, Romay, Maria Cinta, Glaubitz, Jeffrey C., Sun, Qi, Buckler, Edward S., Holland, James B., Doebley, John F.“…Yield (total grain weight) per plant is the sole trait that selection does not appear to have improved in maize relative to teosinte. From a multivariate evolution perspective, we identified a strong, nonneutral divergence between teosinte and maize landrace genetic variance–covariance matrices ([Formula: see text]-matrices). …”
Publicado 2019
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8por Berube, Benjamin, Ernst, Evan, Cahn, Jonathan, Roche, Benjamin, de Santis Alves, Cristiane, Lynn, Jason, Scheben, Armin, Siepel, Adam, Ross-Ibarra, Jeffrey, Kermicle, Jerry, Martienssen, Rob“…Using single molecule and single-pollen genome sequencing, we describe Teosinte Pollen Drive, an instance of gene drive in hybrids between maize (Zea mays ssp. mays) and teosinte mexicana (Zea mays ssp. mexicana), that depends on RNA interference (RNAi). 22nt small RNAs from a non-coding RNA hairpin in mexicana depend on Dicer-Like 2 (Dcl2) and target Teosinte Drive Responder 1 (Tdr1), which encodes a lipase required for pollen viability. …”
Publicado 2023
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9“…Maize (Zea mays ssp. mays) kernel weight has increased more than 10-fold in the 9000 years since domestication from its wild ancestor, teosinte (Z. mays ssp. parviglumis). In order to study how size and shape affect kernel weight, we analyzed kernel morphometric traits in a set of 10 maize-teosinte introgression populations using digital imaging software. …”
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10“…Teosinte (Zea mays ssp. parviglumis) is the wild ancestor of modern maize (Zea mays ssp. mays). …”
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12por Fustier, Margaux-Alison, Martínez-Ainsworth, Natalia E., Aguirre-Liguori, Jonás A., Venon, Anthony, Corti, Hélène, Rousselet, Agnès, Dumas, Fabrice, Dittberner, Hannes, Camarena, María G., Grimanelli, Daniel, Ovaskainen, Otso, Falque, Matthieu, Moreau, Laurence, de Meaux, Juliette, Montes-Hernández, Salvador, Eguiarte, Luis E., Vigouroux, Yves, Manicacci, Domenica, Tenaillon, Maud I.“…Here we focused on adaptation of teosinte populations along two elevation gradients in Mexico that display continuous environmental changes at a short geographical scale. …”
Publicado 2019
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13por Calfee, Erin, Gates, Daniel, Lorant, Anne, Perkins, M. Taylor, Coop, Graham, Ross-Ibarra, Jeffrey“…Here we evaluate these opposing selection forces on introgressed ancestry between maize (Zea mays ssp. mays) and its wild teosinte relative, mexicana (Zea mays ssp. mexicana). …”
Publicado 2021
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14por Rivera-Rodríguez, Diana María, Mastretta-Yanes, Alicia, Wegier, Ana, De la Cruz Larios, Lino, Santacruz-Ruvalcaba, Fernando, Ruiz Corral, José Ariel, Hernández, Benjamín, Sánchez González, José de Jesús“…The wild species of the genus Zea commonly named teosintes, comprise nine different taxa, distributed from northern Mexico to Costa Rica. …”
Publicado 2023
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15Using Association Mapping in Teosinte to Investigate the Function of Maize Selection-Candidate Genes“…METHODS AND FINDINGS: As a step toward defining the traits controlled by these genes, we performed phenotype-genotype association mapping in teosinte for 32 of the 48 plus three other selection-candidate genes. …”
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16por Chavez, Nancy B., Flores, Jose J., Martin, Joseph, Ellstrand, Norman C., Guadagnuolo, Roberto, Heredia, Sylvia, Welles, Shana R.“…Maize x Teosinte Hybrid Cobs Do Not Prevent Crop Gene Introgression. …”
Publicado 2012
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17por Chen, Qiuyue, Samayoa, Luis Fernando, Yang, Chin Jian, Bradbury, Peter J., Olukolu, Bode A., Neumeyer, Michael A., Romay, Maria Cinta, Sun, Qi, Lorant, Anne, Buckler, Edward S., Ross-Ibarra, Jeffrey, Holland, James B., Doebley, John F.“…We observed that large effect QTL have low minor allele frequency (MAF) in both maize and teosinte. Regions of the genome that are strongly differentiated between teosinte and maize (high F(ST)) explain less quantitative variation in maize than teosinte, suggesting that, in these regions, allelic variants were brought to (or near) fixation during domestication. …”
Publicado 2020
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18“…In wheat, genetic control of height has been largely contributed by the Reduced height-1 alleles that confer gibberellin insensitivity; the beneficial effects of these alleles are associated with less favourable effects involving seedling emergence, grain quality, and inflorescence architecture that have driven new research investigating genetic variation of stem growth. Here, we show that TEOSINTE BRANCHED1 (TB1) regulates height of wheat, with TB1 being expressed at low levels in nodes of the main culm prior to elongation, and increased dosage of TB1 restricting elongation of stem internodes. …”
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19por Minow, Mark A A, Ávila, Luis M, Turner, Katie, Ponzoni, Elena, Mascheretti, Iride, Dussault, Forest M, Lukens, Lewis, Rossi, Vincenzo, Colasanti, Joseph“…Temperate maize was domesticated from its tropical ancestor, teosinte. Whereas temperate maize is an autonomous day-neutral plant, teosinte is an obligate short-day plant that requires uninterrupted long nights to induce flowering. …”
Publicado 2018
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20Characterization of introgression from the teosinte Zea mays ssp. mexicana to Mexican highland maizepor Gonzalez-Segovia, Eric, Pérez-Limon, Sergio, Cíntora-Martínez, G. Carolina, Guerrero-Zavala, Alejandro, Janzen, Garrett M., Hufford, Matthew B., Ross-Ibarra, Jeffrey, Sawers, Ruairidh J. H.“…BACKGROUND: The spread of maize cultivation to the highlands of central Mexico was accompanied by substantial introgression from the endemic wild teosinte Zea mays ssp. mexicana, prompting the hypothesis that the transfer of beneficial variation facilitated local adaptation. …”
Publicado 2019
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