TY - JOUR
T1 - Parallel embryonic transcriptional programs evolve under distinct constraints and may enable morphological conservation amidst adaptation
AU - Malik, Assaf
AU - Gildor, Tsvia
AU - Sher, Noa
AU - Layous, Majed
AU - Ben-Tabou de-Leon, Smadar
N1 - Funding Information: We thank Zeev Frenkel for his advice regarding the statistical analysis conducted. We thank Muki Shpigel and David Ben-Ezra for their help with sea urchin handling. We thank the Genomics unit at the Grand Israel National Center for Personalized Medicine (G-INCPM) for their assistance with library preparation and sequencing. We thank Yarden Ben-Tabou de-Leon for the embryo drawings in Fig. 4 . This work was supported by the Israel Science Foundation grants number 41/14 and 2304/15 (ISF-INCPM). Appendix A Funding Information: We thank Zeev Frenkel for his advice regarding the statistical analysis conducted. We thank Muki Shpigel and David Ben-Ezra for their help with sea urchin handling. We thank the Genomics unit at the Grand Israel National Center for Personalized Medicine (G-INCPM) for their assistance with library preparation and sequencing. We thank Yarden Ben-Tabou de-Leon for the embryo drawings in Fig. 4. This work was supported by the Israel Science Foundation grants number 41/14 and 2304/15 (ISF-INCPM). Publisher Copyright: © 2017 Elsevier Inc.
PY - 2017/10/1
Y1 - 2017/10/1
N2 - Embryonic development evolves by balancing stringent morphological constraints with genetic and environmental variation. The design principle that allows developmental transcriptional programs to conserve embryonic morphology while adapting to environmental changes is still not fully understood. To address this fundamental challenge, we compare developmental transcriptomes of two sea urchin species, Paracentrotus lividus and Strongylocentrotus purpuratus, that shared a common ancestor about 40 million years ago and are geographically distant yet show similar morphology. We find that both developmental and housekeeping genes show highly dynamic and strongly conserved temporal expression patterns. The expression of other gene sets, including homeostasis and response genes, show divergent expression which could result from either evolutionary drift or adaptation to local environmental conditions. The interspecies correlations of developmental gene expressions are highest between morphologically similar developmental time points whereas the interspecies correlations of housekeeping gene expression are high between all the late zygotic time points. Relatedly, the position of the phylotypic stage varies between these two groups of genes: developmental gene expression shows highest conservation at mid-developmental stage, in agreement with the hourglass model while the conservation of housekeeping genes keeps increasing with developmental time. When all genes are combined, the relationship between conservation of gene expression and morphological similarity is partially masked by housekeeping genes and genes with diverged expression. Our study illustrates various transcriptional programs that coexist in the developing embryo and evolve under different constraints. Apparently, morphological constraints underlie the conservation of developmental gene expression while embryonic fitness requires the conservation of housekeeping gene expression and the species-specific adjustments of homeostasis gene expression. The distinct evolutionary forces acting on these transcriptional programs enable the conservation of similar body plans while allowing adaption.
AB - Embryonic development evolves by balancing stringent morphological constraints with genetic and environmental variation. The design principle that allows developmental transcriptional programs to conserve embryonic morphology while adapting to environmental changes is still not fully understood. To address this fundamental challenge, we compare developmental transcriptomes of two sea urchin species, Paracentrotus lividus and Strongylocentrotus purpuratus, that shared a common ancestor about 40 million years ago and are geographically distant yet show similar morphology. We find that both developmental and housekeeping genes show highly dynamic and strongly conserved temporal expression patterns. The expression of other gene sets, including homeostasis and response genes, show divergent expression which could result from either evolutionary drift or adaptation to local environmental conditions. The interspecies correlations of developmental gene expressions are highest between morphologically similar developmental time points whereas the interspecies correlations of housekeeping gene expression are high between all the late zygotic time points. Relatedly, the position of the phylotypic stage varies between these two groups of genes: developmental gene expression shows highest conservation at mid-developmental stage, in agreement with the hourglass model while the conservation of housekeeping genes keeps increasing with developmental time. When all genes are combined, the relationship between conservation of gene expression and morphological similarity is partially masked by housekeeping genes and genes with diverged expression. Our study illustrates various transcriptional programs that coexist in the developing embryo and evolve under different constraints. Apparently, morphological constraints underlie the conservation of developmental gene expression while embryonic fitness requires the conservation of housekeeping gene expression and the species-specific adjustments of homeostasis gene expression. The distinct evolutionary forces acting on these transcriptional programs enable the conservation of similar body plans while allowing adaption.
KW - Adaptation
KW - Comparative transcriptomes
KW - Development and evolution
KW - Echinoderms
KW - Gene regulation
KW - Hourglass
UR - http://www.scopus.com/inward/record.url?scp=85026782897&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.ydbio.2017.07.019
DO - https://doi.org/10.1016/j.ydbio.2017.07.019
M3 - Article
C2 - 28780048
SN - 0012-1606
VL - 430
SP - 202
EP - 213
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -