Unravelling cotton RNAseq repositories to the fiber development specific modules and their alliance with the fiber-related traits

Abstract

Cotton fiber development is still an intriguing question to understand the fiber commitment and development. Here, we remapped >350 publicly available cotton RNA sequencing data on recently published cotton genome with ~400 fold coverage. The differentially expressed genes were clustered in six modules whose functions are specific to commitment, initiation, elongation and Secondary Cell Wall (SCW) fiber development stages. Gene Ontology analysis of commitment and initiation specific modules suggests enrichment of genes involved in organ development. The modules specific for elongation and SCW showed significant enrichment of hydroxyproline-rich proteins and hydrolases. Transcription factors (TFs) binding frequency of defined modules suggested that homeodomain, MYB and NAC expresses at commitment stages but their expression was governed by other TFs. We also mined the stage-specific transcriptional biomarker and Exclusively Expressed Transcripts (EETs) for fiber. These EETs were positively selected during fiber evolution and cotton domestication. The extensive expression profiling of six EETs in 100 cotton genotypes at different fiber developmental stages using nCounter assay and their correlation with eight fiber-related suggests that several EETs are correlated with different fiber quality-related traits. Thus, our study reveals several important genes and pathways that may be important for cotton fiber development and future improvement of cotton.

Evolutionary and Functional Characterization of Cytochrome P450 in Cotton Reveal the Role of Subgenome Expression of GhCYP78A for Cotton Fiber Initiation

“…The dual functionality of GhCYP78A has been validated through one of its orthologs, GhCYP78A198_A, whose expression was relatively high at -3 DPA and 21 DPA (Fig. 5A) also reproducing our previous result [54]. In plants, different CYP78A viz., CYP78A5 (KLUH), CYP78A6 (EOD3) and CYP78A7 (PLA1) were functionally characterized for different organ development, cell fate determining and differentiation processes that possibly worked downstream to the GA [12][13][14]52,[55][56][57][58][59][60].…”