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Expansion of the circadian transcriptome in Brassica rapa and genome-wide diversification of paralog expression patterns

View ORCID ProfileKathleen Greenham, View ORCID ProfileRyan C. Sartor, View ORCID ProfileStevan Zorich, View ORCID ProfilePing Lou, View ORCID ProfileTodd C. Mockler, View ORCID ProfileC. Robertson McClung
doi: https://doi.org/10.1101/2020.04.03.024281
Kathleen Greenham
1University of Minnesota
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Ryan C. Sartor
2North Carolina State University
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Stevan Zorich
1University of Minnesota
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Ping Lou
3Dartmouth College
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Todd C. Mockler
4Donald Danforth Plant Science Center
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C. Robertson McClung
3Dartmouth College
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  • For correspondence: c.robertson.mcclung@dartmouth.edu
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Abstract

An important challenge of crop improvement strategies is assigning function to paralogs in polyploid crops. Gene expression is one method for determining the activity of paralogs; however, the majority of transcript abundance data represents a static point that does not consider the spatial and temporal dynamics of the transcriptome. Studies in Arabidopsis have estimated up to 90% of the transcriptome to be under diel or circadian control depending on the condition. As a result, time of day effects on the transcriptome have major implications on how we characterize gene activity. In this study, we aimed to resolve the circadian transcriptome in the polyploid crop Brassica rapa and explore the fate of multicopy orthologs of Arabidopsis circadian regulated genes. We performed a high-resolution time course study with 2 h sampling density to capture the genes under circadian control. Strikingly, more than two-thirds of expressed genes exhibited rhythmicity indicative of circadian regulation. To compare the expression patterns of paralogous genes, we developed a program in R called DiPALM (Differential Pattern Analysis by Linear Models) that analyzes time course data to identify transcripts with significant pattern differences. Using DiPALM, we identified genome-wide divergence of expression patterns among retained paralogs. Cross-comparison with a previously generated diel drought experiment in B. rapa revealed evidence for differential drought response for these diverging paralog pairs. Using gene regulatory network models we compared transcription factor targets between B. rapa and Arabidopsis circadian networks to reveal additional evidence for divergence in expression between B. rapa paralogs that may be driven in part by variation in conserved non coding sequences. These findings provide new insight into the rapid expansion and divergence of the transcriptional network in a polyploid crop and offer a new method for assessing paralog activity at the transcript level.

Significance The circadian regulation of the transcriptome leads to time of day changes in gene expression that coordinates environmental conditions with physiological responses. Brassica rapa, a morphologically diverse crop species, has undergone whole genome triplication since diverging from Arabidopsis resulting in an expansion of gene copy number. To examine how this expansion has influenced the circadian transcriptome we developed a new method for comparing gene expression patterns. This method facilitated the discovery of genome-wide expansion of expression patterns for genes present in multiple copies and divergence in temporal abiotic stress response. We find support for conserved sequences outside the gene body contributing to these expression pattern differences and ultimately generating new connections in the gene regulatory network.

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Posted April 05, 2020.
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Expansion of the circadian transcriptome in Brassica rapa and genome-wide diversification of paralog expression patterns
Kathleen Greenham, Ryan C. Sartor, Stevan Zorich, Ping Lou, Todd C. Mockler, C. Robertson McClung
bioRxiv 2020.04.03.024281; doi: https://doi.org/10.1101/2020.04.03.024281
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Expansion of the circadian transcriptome in Brassica rapa and genome-wide diversification of paralog expression patterns
Kathleen Greenham, Ryan C. Sartor, Stevan Zorich, Ping Lou, Todd C. Mockler, C. Robertson McClung
bioRxiv 2020.04.03.024281; doi: https://doi.org/10.1101/2020.04.03.024281

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