skip to main content


Title: Changes in chromatin accessibility between Arabidopsis stem cells and mesophyll cells illuminate cell type‐specific transcription factor networks
Summary

Cell differentiation is driven by changes in the activity of transcription factors (TFs) and subsequent alterations in transcription. To study this process, differences inTFbinding between cell types can be deduced by probing chromatin accessibility. We used cell type‐specific nuclear purification followed by the assay for transposase‐accessible chromatin (ATAC‐seq) to delineate differences in chromatin accessibility andTFregulatory networks between stem cells of the shoot apical meristem (SAM) and differentiated leaf mesophyll cells inArabidopsis thaliana. Chromatin accessibility profiles ofSAMstem cells and leaf mesophyll cells were very similar at a qualitative level, yet thousands of regions having quantitatively different chromatin accessibility were also identified. Analysis of the genomic regions preferentially accessible in each cell type identified hundreds of overrepresentedTF‐binding motifs, highlighting sets ofTFs that are probably important for each cell type. Within these sets, we found evidence for extensive co‐regulation of target genes by multipleTFs that are preferentially expressed in each cell type. Interestingly, theTFs within each of these cell type‐enriched sets also showed evidence of extensively co‐regulating each other. We further found that preferentially accessible chromatin regions in mesophyll cells tended to also be substantially accessible in the stem cells, whereas the converse was not true. This observation suggests that the generally higher accessibility of regulatory elements in stem cells might contribute to their developmental plasticity. This work demonstrates the utility of cell type‐specific chromatin accessibility profiling for the rapid development of testable models of regulatory control differences between cell types.

 
more » « less
PAR ID:
10056086
Author(s) / Creator(s):
 ;  ;  ;  ;  
Publisher / Repository:
Wiley-Blackwell
Date Published:
Journal Name:
The Plant Journal
Volume:
94
Issue:
2
ISSN:
0960-7412
Page Range / eLocation ID:
p. 215-231
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Summary

    The shoot stem cell niche, contained within the shoot apical meristem (SAM) is maintained in Arabidopsis by the homeodomain proteinSHOOT MERISTEMLESS(STM).STMis a mobile protein that traffics cell‐to‐cell, presumably through plasmodesmata. In maize, theSTMhomologKNOTTED1 shows clear differences betweenmRNAand protein localization domains in theSAM. However, theSTM mRNAand protein localization domains are not obviously different in Arabidopsis, and the functional relevance ofSTMmobility is unknown. Using a non‐mobile version ofSTM(2xNLSYFPSTM), we show thatSTMmobility is required to suppress axillary meristem formation during embryogenesis, to maintain meristem size, and to precisely specify organ boundaries throughout development.STMand organ boundary genesCUP SHAPED COTYLEDON1(CUC1),CUC2andCUC3regulate each other during embryogenesis to establish the embryonicSAMand to specify cotyledon boundaries, andSTMcontrolsCUCexpression post‐embryonically at organ boundary domains. We show that organ boundary specification by correct spatial expression ofCUCgenes requiresSTMmobility in the meristem. Our data suggest thatSTMmobility is critical for its normal function in shoot stem cell control.

     
    more » « less
  2. Summary

    Mesophyll conductance (gm) is the diffusion ofCO2from intercellular air spaces (IAS) to the first site of carboxylation in the mesophyll cells. In C3species,gmis influenced by diverse leaf structural and anatomical traits; however, little is known about traits affectinggmin C4species.

    To address this knowledge gap, we used online oxygen isotope discrimination measurements to estimategmand microscopy techniques to measure leaf structural and anatomical traits potentially related togmin 18 C4grasses.

    In this study,gmscaled positively with photosynthesis and intrinsic water‐use efficiency (TEi), but not with stomatal conductance. Also,gmwas not determined by a single trait but was positively correlated with adaxial stomatal densities (SDada), stomatal ratio (SR), mesophyll surface area exposed toIAS(Smes) and leaf thickness. However,gmwas not related to abaxial stomatal densities (SDaba) and mesophyll cell wall thickness (TCW).

    Our study suggests that greaterSDadaandSRincreasedgmby increasingSmesand creating additional parallel pathways forCO2diffusion inside mesophyll cells. Thus,SDada,SRandSmesare important determinants of C4gmand could be the target traits selected or modified for achieving greatergmandTEiin C4species.

     
    more » « less
  3. Summary

    Here we report the expression of programmed cell death ligand 1/2 (PD‐L1/L2) in breast and colon cancer stem cells (CSCs). The stemness of these cells was confirmed by their surface markers. Using flow cytometry analysis we demonstrated thatPD‐L1 expression was higher inCSCs of both cancers compared to non‐stem like cancer cells. Consistent with this, detection of cellularPD‐L1 proteins by western blot assay also showed increasedPD‐L1 protein inCSCs. In contrast, only trace amounts ofPD‐L2 were detected inCSCs of both cancers. Our results suggest that breast and colon cancers may be sensitive toPD1/PD‐L1 immunotherapy and thus warrant further investigations ofCSCtargetedPD1/PD‐L1 therapy.

     
    more » « less
  4. Summary

    B‐cell responses are dynamic processes that depend on multiple types of interactions. Rare antigen‐specific B cells must encounter antigen and specialized systems are needed—unique to each lymphoid tissue type—to ensure this happens efficiently. Lymphoid tissue barrier cells act to ensure that pathogens, while being permitted entry for B‐cell recognition, are blocked from replication or dissemination. T follicular helper (Tfh) cells often need to be primed by dendritic cells before supporting B‐cell responses. For most responses, antigen‐specific helper T cells and B cells need to interact, first to initiate clonal expansion and the plasmablast response, and later to support the germinal center (GC) response. Newly formed plasma cells need to travel to supportive niches.GCB cells must become confined to the follicle center, organize into dark and light zones, and interact with Tfh cells. Memory B cells need to be positioned for rapid responses following reinfection. Each of these events requires the actions of multiple G‐protein coupled receptors (GPCRs) and their ligands, including chemokines and lipid mediators. This review will focus on the guidance cue code underlying B‐cell immunity, with an emphasis on findings from our laboratory and on newer advances in related areas. We will discuss our recent identification of geranylgeranyl‐glutathione as a ligand for P2RY8. Our goal is to provide the reader with a focused knowledge about theGPCRs guiding B‐cell responses and how they might be therapeutic targets, while also providing examples of how multiple types ofGPCRs can cooperate or act iteratively to control cell behavior.

     
    more » « less
  5. Red algae are the oldest identifiable multicellular eukaryotes, with a fossil record dating back more than a billion years. During that time two major rhodophyte lineages, bangiophytes and florideophytes, have evolved varied levels of morphological complexity. These two groups are distinguished, in part, by different patterns of multicellular development, with florideophytes exhibiting a far greater diversity of morphologies. Interestingly, during their long evolutionary history, there is no record of a rhodophyte achieving the kinds of cellular and tissue‐specific differentiation present in other multicellular algal lineages. To date, the genetic underpinnings of unique aspects of red algal development are largely unexplored; however, they must reflect the complements and patterns of expression of key regulatory genes. Here we report comparative evolutionary and gene expression analyses of core subunits of theSWI/SNFchromatin‐remodeling complex, which is implicated in cell differentiation and developmental regulation in more well studied multicellular groups. Our results suggest that a single, canonicalSWI/SNFcomplex was present in the rhodophyte ancestor, with gene duplications and evolutionary diversification ofSWI/SNFsubunits accompanying the evolution of multicellularity in the common ancestor of bangiophytes and florideophytes. Differences in howSWI/SNFchromatin remodeling evolved subsequently, in particular gene losses and more rapid divergence ofSWI3 andSNF5 in bangiophytes, could help to explain why they exhibit a more limited range of morphological complexity than their florideophyte cousins.

     
    more » « less