IAL   21557
INSTITUTO DE AGROBIOTECNOLOGIA DEL LITORAL
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Sequence characterization and expression analysis of peaunut (Arachis hypogea) lncRNA Enod40 (AhEnod40)
Autor/es:
WANG, J.; TONELLI, M.L.; RODRIGUEZ, JOHAN; ARIEL, FEDERICO D.; FARBRA, A.; PENG, Z.; LUCERO LEANDRO E.; IBAÑEZ, FERNANDO
Reunión:
Workshop; Biología Celular y Molecular del ARN; 2018
Resumen:
Peanut (Arachis hypogaea L.) is an important legume crop worldwide. It is an allotetraploid species (2n=4x=40, AABB genome type; about 2.8 Gb with a high repetitive DNA content) probably derived from a singlehybridization event of two wild species, A. ipaënsis and A. duranensis (2n=20). The complexity of cultivated peanut genome has hindered its sequencing. Therefore, only the genomic sequence of the wild peanutancestors was available in databases until very recently.As a legume, peanut is able to interact with bradyrhizobia in a nitrogen-fixing symbiosis. In peanut, symbiotic development occurs through a primitive and poorly characterized aeschynomenoid program. Relativelylittle is known about the molecules implicated in this symbiotic process. Enod40 is a classic early nodulin reported as essential for nodulation in several legumes. This long non-coding RNA (lncRNA) has an unusualstructure, since it lacks a long open reading frame (ORF). However, short ORFs are present (Sousa et al., 2001) in Enod40 transcripts, coding for two peptides apparently linked to its biological activity. Due to thehighly structured RNA, it has been suggested that the Enod40 activity resides in the RNA (Crespi et al., 1994; Sousa et al., 2001; Girard et al., 2003). It has also been reported that Enod40 participates in thenucleocytoplasmic trafficking of RBP1 and in RBP1-dependent splicing modulation ( Crespi et al., 1994; Campalans et al., 2004; Romero-Barrios et al., 2018).In a previous work (Peng et al., 2017), regions XLOC_021512 and XLOC_058301 were identified as upregulated in four nod+ peanut lines tested during the establishment of N-fixing symbiosis (5 dpi). However,these chromosomic regions were not further characterized. In this work, we provide evidence that these regions encode for Enod40 and analyse the transcript folding predictions and expression patterns duringearly time points of symbiotic development.