TY - JOUR
T1 - Transcriptome dynamics of the stomatal lineage
T2 - Birth, amplification, and termination of a self-renewing population
AU - Adrian, Jessika
AU - Chang, Jessica
AU - Ballenger, Catherine E.
AU - Bargmann, Bastiaan O R
AU - Alassimone, Julien
AU - Davies, Kelli A.
AU - Lau, On Sun
AU - Matos, Juliana L.
AU - Hachez, Charles
AU - Lanctot, Amy
AU - Vatén, Anne
AU - Birnbaum, Kenneth D.
AU - Bergmann, Dominique C.
N1 - Funding Information:
We thank Ligeng Ma and Martin Hülskamp for reagents, Tie Liu for initial FACS protocols, Trevor Martin for statistics consulting, José Dinneny and Xueliang Wei for eFP browser compatible files, and members of our laboratory for critical comments. Funding for this work was provided by NIH 1R01GM086632. J. Adrian was supported by a fellowship from the German Academic Exchange Service; K.A.D. was supported by Training Program NIH5T32GM007276 and by an NSF graduate research fellowship. O.S.L. was a Croucher Fellow. J. Alassimone was supported by an Early PostDoc Mobility fellowship from the Swiss National Science Foundation and by an EMBO Long-term Fellowship; C.H. was funded by the Belgian American Educational Foundation and the Belgian National Fund for Scientific Research. D.C.B. is a Gordon and Betty Moore Foundation Investigator of the Howard Hughes Medical Institute. Sorting was performed at the Stanford Shared FACS Facility supported by an NIH Shared Instrument Grant (S10RR025518-01). The Vincent J. Coates Genomics Sequencing Laboratory at UC Berkeley was supported by NIH Instrumentation Grants S10RR029668 and S10RR027303.
Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/4/6
Y1 - 2015/4/6
N2 - Developmental transitions can be described in terms of morphology and the roles of individual genes, butalso in terms of global transcriptional and epigenetic changes. Temporal dissections of transcriptome changes, however, are rare for intact, developing tissues. We used RNA sequencing and microarray platforms to quantify gene expression from labeled cells isolated by fluorescence-activated cell sorting to generate cell-type-specific transcriptomes during development of an adult stem-cell lineage in the Arabidopsis leaf. We show that regulatory modules in this early lineage link cell types that hadpreviously been considered to be under separate control and provide evidence for recruitment ofindividual members of gene families for different developmental decisions. Because stomata are physiologically important and because stomatal lineage cells exhibit exemplary division, cell fate, and cell signaling behaviors, this dataset serves as a valuable resource for further investigations of fundamental developmental processes.
AB - Developmental transitions can be described in terms of morphology and the roles of individual genes, butalso in terms of global transcriptional and epigenetic changes. Temporal dissections of transcriptome changes, however, are rare for intact, developing tissues. We used RNA sequencing and microarray platforms to quantify gene expression from labeled cells isolated by fluorescence-activated cell sorting to generate cell-type-specific transcriptomes during development of an adult stem-cell lineage in the Arabidopsis leaf. We show that regulatory modules in this early lineage link cell types that hadpreviously been considered to be under separate control and provide evidence for recruitment ofindividual members of gene families for different developmental decisions. Because stomata are physiologically important and because stomatal lineage cells exhibit exemplary division, cell fate, and cell signaling behaviors, this dataset serves as a valuable resource for further investigations of fundamental developmental processes.
UR - http://www.scopus.com/inward/record.url?scp=84926313481&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84926313481&partnerID=8YFLogxK
U2 - 10.1016/j.devcel.2015.01.025
DO - 10.1016/j.devcel.2015.01.025
M3 - Article
C2 - 25850675
AN - SCOPUS:84926313481
SN - 1534-5807
VL - 33
SP - 107
EP - 118
JO - Developmental Cell
JF - Developmental Cell
IS - 1
ER -