Análisis de una cartera de extensión agrícola para sorgo (Sorghum bicolor L. Moench) en los estados Barinas y Portuguesa, Venezuela.

La presente investigación tuvo como objetivo evaluar el rendimiento y riesgo que presenta la cartera de fincas productoras de sorgo, en los estados Portuguesa y Barinas (Venezuela), adscritas al Programa de Extensión Agrícola Italven S. A. (PEAISA). La muestra fue conformada por 39 fincas localizadas en tres municipios del estado Portuguesa y 72 fincas ubicadas en siete municipios del estado Barinas. En todas se produjo sorgo, a la salida de lluvias, durante 2006. Se consideraron las variables estado, municipio, área cosechada, híbridos cultivados, rendimiento y coeficiente de variación (riesgo). Se empleó distribución de frecuencias de la superficie cosechada de sorgo por finca para medir la concentración de la cartera y se realizaron comparaciones de promedio de rendimiento con las pruebas de t de student y de Tukey, además se utilizó la curva normal para determinar probabilidades de rendimiento. Entre los resultados más importantes destacan: 1) La cartera del PEAISA, conformada por fincas pequeñas y medianas, no presenta riesgo de concentración en un determinado segmento de tamaño, pero la producción total está concentrada (81,2%) en el estado Barinas, 2) Aunque se ubicó en la media nacional, se logró un mayor rendimiento promedio/ha de sorgo en el estado Barinas en comparación con Portuguesa, con riesgo de explotación similar en ambos estados, 3) El híbrido de sorgo Tecsen 120 igualó al Chaguarama VII, pero superó en rendimiento al Himeca 101, híbrido que pudiera ser descartado de la cartera por su bajo rendimiento y mayor riesgo de explotación. Esta información se analizó adicionalmente con una matriz denominada productividad-riesgo, que fue un desarrollo original de este trabajo.

Cell type-specific loss of atp6 RNA editing in cytoplasmic male sterile Sorghum bicolor

RNA editing and cytoplasmic male sterility are two important phenomena in higher plant mitochondria. To determine whether correlations might exist between the two, RNA editing in different tissues of Sorghum bicolor was compared employing reverse transcription–PCR and subsequent sequence analysis. In etiolated shoots, RNA editing of transcripts of plant mitochondrial atp6, atp9, nad3, nad4, and rps12 genes was identical among fertile or cytoplasmic male sterile plants. We then established a protocol for mitochondrial RNA isolation from plant anthers and pollen to include in these studies. Whereas RNA editing of atp9, nad3, nad4, and rps12 transcripts in anthers was similar to etiolated shoots, mitochondrial atp6 RNA editing was strongly reduced in anthers of the A3Tx398 male sterile line of S. bicolor. atp6 transcripts of wheat and selected plastid transcripts in S. bicolor showed normal RNA editing, indicating that loss of atp6 RNA editing is specific for cytoplasmic male sterility S. bicolor mitochondria. Restoration of fertility in F1 and F2 lines correlated with an increase in RNA editing of atp6 transcripts. Our data suggest that loss of atp6 RNA editing contributes to or causes cytoplasmic male sterility in S. bicolor. Further analysis of the mechanism of cell type-specific loss of atp6 RNA editing activity may advance our understanding of the mechanism of RNA editing.

Molecular characterization of a mutable pigmentation phenotype and isolation of the first active transposable element from Sorghum bicolor

Accumulation of red phlobaphene pigments in sorghum grain pericarp is under the control of the Y gene. A mutable allele of Y, designated as y-cs (y-candystripe), produces a variegated pericarp phenotype. Using probes from the maize p1 gene that cross-hybridize with the sorghum Y gene, we isolated the y-cs allele containing a large insertion element. Our results show that the Y gene is a member of the MYB-transcription factor family. The insertion element, named Candystripe1 (Cs1), is present in the second intron of the Y gene and shares features of the CACTA superfamily of transposons. Cs1 is 23,018 bp in size and is bordered by 20-bp terminal inverted repeat sequences. It generated a 3-bp target site duplication upon insertion within the Y gene and excised from y-cs, leaving a 2-bp footprint in two cases analyzed. Reinsertion of the excised copy of Cs1 was identified by Southern hybridization in the genome of each of seven red pericarp revertant lines tested. Cs1 is the first active transposable element isolated from sorghum. Our analysis suggests that Cs1-homologous sequences are present in low copy number in sorghum and other grasses, including sudangrass, maize, rice, teosinte, and sugarcane. The low copy number and high transposition frequency of Cs1 imply that this transposon could prove to be an efficient gene isolation tool in sorghum.