The floral development of the allotetraploid Coffea arabica L. correlates with a small RNA dynamic reprogramming.
Thales Henrique Cherubino RibeiroPatricia BaldrichRaphael Ricon de OliveiraChristiane Noronha Fernandes-BrumSandra Marisa MathioniThaís Cunha de Sousa CardosoMatheus de Souza GomesLaurence Rodrigues do AmaralKellen Kauanne Pimenta de OliveiraGabriel Lasmar Dos ReisBlake C MeyersAntonio Chalfun-JuniorPublished in: The Plant journal : for cell and molecular biology (2024)
Noncoding and coding RNAs are key regulators of plant growth, development, and stress responses. To investigate the types of transcripts accumulated during the vegetative to reproductive transition and floral development in the Coffea arabica L., we sequenced small RNA libraries from eight developmental stages, up to anthesis. We combined these data with messenger RNA and PARE sequencing of two important development stages that marks the transition of an apparent latent to a rapid growth stage. In addition, we took advantage of multiple in silico tools to characterize genomic loci producing small RNAs such as phasiRNAs, miRNAs, and tRFs. Our differential and co-expression analysis showed that some types of small RNAs such as tRNAs, snoRNAs, snRNAs, and phasiRNAs preferentially accumulate in a stage-specific manner. Members of the miR482/miR2118 superfamily and their 21-nucleotide phasiRNAs originating from resistance genes show a robust co-expression pattern that is maintained across all the evaluated developmental stages. Finally, the majority of miRNAs accumulate in a family stage-specific manner, related to modulated hormonal responses and transcription factor expression.
Keyphrases
- transcription factor
- poor prognosis
- cell proliferation
- long non coding rna
- genome wide identification
- long noncoding rna
- magnetic resonance imaging
- type diabetes
- magnetic resonance
- gene expression
- molecular docking
- adipose tissue
- big data
- copy number
- polycystic ovary syndrome
- artificial intelligence
- molecular dynamics simulations
- dna binding
- contrast enhanced