Repositorio Fedepalma

A marker-based strategy for the assessment of epigenetic instability in oil palm.

dc.creatorPIPOC 2007 International Palm Oil Congress Palm oil: Empowering change
dc.creatorBeulé, Thierry
dc.creatorFinnegan, E. Jean
dc.creatorJaligot, Estelle
dc.creatorRival, Alain
dc.creatorTregear, James
dc.creatorMalaysian Palm Oil Board, MPOB
dc.date2007.
dc.descriptionPlant tissues from the mantled somaclonal variant of oil palm have been found to display both large-scale perturbations of genomic methylation levels and sequence-specific DNA methylation pattern changes when compared to their true-to-type counterparts. Concomitantly, several markers showing phenotype-specific transcription patterns have been identified in our group. Some of them are likely to be indicators of the altered physiological state of abnormal cultures, others are possible targets of epigenetic misregulations of flower development. We now aim to establish the exact link between the expression of these candidate marker genes and the mantled somaclonal variation state, through the exploration of their global epigenetic behaviour. This will be achieved using three complementary approaches applied to normal and abnormal tissues: i) the evaluation of transcription levels through quantitative or semi-quantitative techniques (semi-quantitative RT-PCR, real-time PCR); ii) the determination of sequence-wide DNA methylation patterns (bisulfite sequencing) and iii) the identification of the chromatin regulatory environment of these genes (Chromatin Immuno-Precipitation: ChIP). These combined strategies will ultimately help to elucidate the epigenetic mechanisms which give rise to the mantled somaclonal variant. Also, we will be able to identify which of the candidate markers which are indeed consistently linked with the abnormal state. This work will provide the basis for a molecular detection test of the variant phenotype.
dc.descriptionIncluye referencias bibliográficas.
dc.descriptionPlant tissues from the mantled somaclonal variant of oil palm have been found to display both large-scale perturbations of genomic methylation levels and sequence-specific DNA methylation pattern changes when compared to their true-to-type counterparts. Concomitantly, several markers showing phenotype-specific transcription patterns have been identified in our group. Some of them are likely to be indicators of the altered physiological state of abnormal cultures, others are possible targets of epigenetic misregulations of flower development. We now aim to establish the exact link between the expression of these candidate marker genes and the mantled somaclonal variation state, through the exploration of their global epigenetic behaviour. This will be achieved using three complementary approaches applied to normal and abnormal tissues: i) the evaluation of transcription levels through quantitative or semi-quantitative techniques (semi-quantitative RT-PCR, real-time PCR); ii) the determination of sequence-wide DNA methylation patterns (bisulfite sequencing) and iii) the identification of the chromatin regulatory environment of these genes (Chromatin Immuno-Precipitation: ChIP). These combined strategies will ultimately help to elucidate the epigenetic mechanisms which give rise to the mantled somaclonal variant. Also, we will be able to identify which of the candidate markers which are indeed consistently linked with the abnormal state. This work will provide the basis for a molecular detection test of the variant phenotype.
dc.identifier.urlhttps://catalogo.fedepalma.org/cgi-bin/koha/opac-detail.pl?biblionumber=20594
dc.languageng
dc.publisherKuala Lumpur : MPOB,
dc.subjectPalma de aceite
dc.titleA marker-based strategy for the assessment of epigenetic instability in oil palm.
dc.typetext

Archivos

Colecciones

Con el Apoyo del Fondo de Fomento Palmero

Calle 98 No. 70 - 91 Pisos 14 y 15
Centro Empresarial Pontevedra
PBX: (+57) 601 - 313 8600 Ext. 1500 - 1501
cidpalmero@fedepalma.org

Horario de atención: Lunes a viernes de 8:00am a 12:00am y de 2:00pm a 4:00pm


Sitio en DSpace implementado por:

Desplegado por Biteca