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R. 1991. Heterochromatin and genome size in Fortunatia and Camassia (Hyacinthaceae). Kew Bulletin, 46, 307-316. , Zabel P. H. 1996. Highresolution physical mapping in Arabidopsis thaliana and tomato by fluorescence in situ hybridization to extended DNA fibers. The Plant Journal, 9, 421-430. A. V. 2007. A method for cellular localization of gene expression via quantitative in situ hybridization in plants. The Plant Journal, 50, 159-175. L. C. 2008. Gene expression analysis at the onset of aposporous apomixis in Paspalum notatum.

Los estudios Biotecnología y Mejoramiento Vegetal II de los nódulos de recombinación en complejos sinaptonémicos han revelado que la discrepancia entre los mapas físicos y genéticos es el resultado de la distribución no al azar de los eventos de crossing-over a lo largo de los cromosomas. En este marco, el desarrollo de los mapas cromosómicos ha cobrado importancia debido a que, dependiendo de las regiones cromosómicas que se analicen y a la frecuencia de recombinación propia de cada una, los mapas genéticos pueden ser mejores o peores estimadores de las distancias físicas reales.

El agente gelificante más utilizado en el cultivo in vitro es el agar, extraído de diversas algas marinas. Las diferentes calidades existentes en el mercado modifican la expresión morfogénica debido a que pueden contener sustancias inhibitorias o promotoras del crecimiento. Tal es el caso del cultivo de hojas de Actinidia chilensis (en medio de MS con el agregado de 0,1 mg/L de AIA + 1 mg/L de BAP) cuya respuesta morfogénica varió según el tipo de agar utilizado. Cuando el gelificante empleado fue Chubut-agar, de producción nacional, se observó una gran diferenciación de yemas adventicias, mientras que con el agregado de agar SIGMA R sólo se indujo la proliferación de callo.

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