- Open Access
Cell type-specific characterization of nuclear DNA contents within complex tissues and organs
© Zhang et al; licensee BioMed Central Ltd. 2005
- Received: 24 August 2005
- Accepted: 04 October 2005
- Published: 04 October 2005
Eukaryotic organisms are defined by the presence of a nucleus, which encloses the chromosomal DNA, and is characterized by its DNA content (C-value). Complex eukaryotic organisms contain organs and tissues that comprise interspersions of different cell types, within which polysomaty, endoreduplication, and cell cycle arrest is frequently observed. Little is known about the distribution of C-values across different cell types within these organs and tissues.
We have developed, and describe here, a method to precisely define the C-value status within any specific cell type within complex organs and tissues of plants. We illustrate the application of this method to Arabidopsis thaliana, specifically focusing on the different cell types found within the root.
The method accurately and conveniently charts C-value within specific cell types, and provides novel insight into developmental processes. The method is, in principle, applicable to any transformable organism, including mammals, within which cell type specificity of regulation of endoreduplication, of polysomaty, and of cell cycle arrest is suspected.
- Transgenic Plant
- Green Fluorescent Protein
- Specific Cell Type
- Green Fluorescent Protein Expression
- Green Fluorescent Protein Fluorescence
The amount of DNA contained within a haploid nucleus of eukaryotic organisms is termed the C (constant) value . For many eukaryotes, the nuclei of somatic cells contain a 2C DNA amount, and the growing cells participate in a simple mitotic cell cycle in which four temporally-linked phases, G1, S, G2 and M, serve to separate the processes of DNA duplication (S-phase) from chromosomal segregation (M-phase). Monosomatic tissues containing mitotically active cells therefore are characterized by cells having nuclear DNA contents ranging from 2C to 4C, depending on the position of the cells within the cell cycle. The proportions of cells within these phases is a function of the proportions of cells that are actively cycling and the degree of cycle synchrony, and evidently reflects also whether or not the cells are arrested at particular points within the cell cycle, most commonly G0/G1 (2C) or G2 (4C). In polysomatic tissues, the situation is complicated by the occurrence of an alternative cell cycle, termed endoreduplication, in which successive S-phases are not followed by M-phases. This produces uninucleate cells having multiplicative DNA contents (2n C, where n = 1,2,3..., for most sources of somatic cells, and 3 × 2n-1 C for the endoreduplicated endosperm derived from triploid progenitor cells). Polysomaty is particularly common in higher plants ; for some species, such as A. thaliana, it is encountered throughout the mature tissues of the organism , while in others it is restricted to specific tissues .
The functional significance of the state of the nuclear C-value at which DNA synthesis arrests remains obscure, in part due to a lack of facile and precise methods for identifying its occurrence as a function of specific cell types. It is clear that, in the analysis of developmental gene expression and the cell biology underlying its regulation, the nuclear C-value represents an important parameter reflecting both the cell cycle status of the cell within which the nucleus is located, as well as the participation of the cells of polysomatic tissues within cycles of endoreduplication. Conversely, the regulated arrest of the cell at specific nuclear C-values reflects the activities of regulatory mechanisms about which we know very little.
We wondered if our flow cytometric methods for analysis of nuclear C-values  might be combined with transgenic expression of a nuclear-targeted version of the Green Fluorescent Protein (GFP) placed under the regulation of cell type-specific promoters, thereby permitting analysis of the C-value status of specific cell types. We reasoned that the labeling of nuclei of specific cell types with GFP would allow their detection using flow cytometry and, via simultaneous biparametric analysis of DNA content, lead to their assignment to various C-value classes. In this report, we validate this experimental approach, describing recombinant DNA constructions that encode Fluorescent Protein (FP)-fusions that are appropriately targeted to the nucleus, and which are quantitatively retained within the nuclei following cell homogenization. We go on to describe conditions for confocal examination of transgenic plants exhibiting a number of different cell-type specific patterns of expression, and for flow cytometric analysis of homogenates prepared from these plants. We finally employ the method to uncover evidence of cell type-specific arrest of particular cell types within different C-value states. The significance of these observations is discussed.
The proposed experimental concept requires that it be possible to target GFP, or other Fluorescent Proteins, to the nuclei of transgenic plants under the control of cell type-specific promoters, that the nuclei display sufficient fluorescent signal to be detectable by microscopy and flow cytometry, that the GFP-based signal not interfere with counterstaining and flow analysis of nuclear DNA content, and that the GFP-based fluorescence be retained within the nuclei following homogenization and during flow analysis. To be maximally useful, the concept and the procedures should be applicable to plants having small (cf. A. thaliana) as well as larger genomes.
The described method relies on the targeting of GFP to the nucleus, and its retention within the nucleus during cellular homogenization and flow cytometric analysis. In previous work, we described the use of a tobacco nuclear localization signal to target a chimeric protein comprising the complete coding region of β-glucuronidase fused to GFP [11, 12]. Although such a molecule is effectively targeted to the nucleoplasm in vivo, it appears to slowly leak out of nuclei following homogenization. This is not an issue for the flow cytometric analysis of nuclei having large DNA contents, such as tobacco, since the nuclear GFP signal remains well above the background detection level of the flow cytometer for reasonable periods of time following homogenization . In contrast, for plants having small nuclear genome sizes, such as A. thaliana, the small size of the nuclei and the low amplitude of the GFP-signal, coupled to leakage of the targeted molecules, means that nucleoplasmic targeting is unsuitable for flow cytometric analysis of isolated nuclei. This problem can be avoided by employing as the targeting signal a nuclear protein that represents a structural component of the nucleus, in this case histone HTA6. Constitutive transgenic expression of the HTA6-GFP fusion protein has no detectable effect upon plant growth or development. Interestingly, constitutive expression of the GFP-HTA6 (i.e. in a reversed orientation) fusion protein also had no perceptible effects on growth and development (data not shown). This is consistent with our understanding of the three-dimensional structures of histones . For HTA6, both the N- and C-termini are exposed at the nucleosomal surface and, of the 13 predicted A. thaliana H2A proteins (HTA; http://www.chromdb.org), HTA6 has the second longest N-terminus (14 aa), and the longest C-terminus (21 aa).
The patterns observed within the two-dimensional frequency distributions produced by flow cytometry indicate that a majority of the root cells of transgenic plants contain green fluorescent nuclei, which confirms that the CaMV 35S promoter is active during the development of the different cell types present within the region analyzed . The fact that HTA6-GFP fluorescence scales linearly and very precisely with DNA content implies the accumulation of nuclear histone 2A is tightly correlated with DNA content. This observation, coupled to the lack of leakage of HTA6-GFP from the nuclei in homogenates, is consistent with the hypothesis that most of the HTA6-GFP is complexed within chromatin rather than being free within the nucleoplasm.
Although the two-dimensional frequency distributions provide unambiguous identification of the DNA content values of GFP-labelled nuclei, for these to be meaningful, it is crucial that expression of HTA6-GFP not perturb the system under study. As far as we can tell, this appears to be the case: no phenotypical differences were seen between transgenic and wild-type plants, nor were differences seen in the proportions of nuclei within the various C-value categories. It should be noted that the same flow cytometric strategy should be technically applicable to transgenic plants expressing any GFP (or other FP) fusion that is targeted to and retained within the nucleus, with the same caveat that such expression not perturb the system under study.
The observation of cell type-specific patterns of C-value suggests that increasing nuclear DNA content represents one strategy evolved by multicellular organisms to specify cell types. As far as we are aware, this is the most precise experimental evidence supporting this rather simple idea in higher plants, and application of this method to other situations in which increased DNA content is associated with cell type differentiation should rapidly provide a valuable body of data. For example, in other work, it has been hypothesized that basal cells within the xylem pericycle cells arrest in G2, thereby becoming susceptible to auxin-mediated signals that trigger the first formative divisions leading to lateral root initiation [15–18]. Consistent with this hypothesis, genes characteristic of the G2/M boundary are coordinately induced in A. thaliana shortly after imposition of conditions leading to synchronized induction of lateral roots .
In both of these situations, cell type specification appears associated with an increase in the proportion of cells containing 4C nuclei. At the cytological level of analysis, such a situation can arise through G2 arrest of cells within a monosomatic diploid cell cycle, or, equally-well, through G1 arrest of cells that have entered the first endoreduplicative cell cycle (i.e. having become tetraploid). Complicating cytological analysis is the potential for formation of polytene chromosomes. Further experiments will evidently be required to clarify the situation, and methods of in situ hybridization utilizing endogenous [19–22] and transgenic chromosomal markers  should prove invaluable.
At the molecular level, many candidates for cell cycle regulators responsible for accumulation of 4C cells can be identified from the existing body of knowledge for other eukaryotic organisms [24, 25], and that emerging for plants, particularly A. thaliana. These include cyclins that are specifically active during the G2/M transition , mitotic cyclin-dependent kinase and its activators and inhibitors [27–34], the anaphase promoting complex (APC) and components that interact with the APC [24, 35, 36], and molecules associated with check-points relating to cell size [37, 38], radiation damage [36, 39], and spindle assembly .
The mechanisms regulating cell cycle status and nuclear DNA content within the endodermal and cortical cells may also reflect the nature of the SCR and SHR genes, which encode members of the GRAS-STAT family of transcription factors [40, 41]. Other members of this family have been shown to interact with regulators of the cell cycle [42–44]. One role of SHR and/or SCR may be to arrest the diploid cell cycle within endodermal cells at the G2/M boundary, and perhaps also to regulate an endoreduplicative event converting these nuclei from a G2 to a G1 state without an intervening M-phase. Of the 30 genes found to be most strongly up- or down-regulated within the endodermis , one candidate for a regulatory role is At5g26900, since it exhibits homology to fizzy1 of X. laevis which is required for APC activation in that system .
Interestingly, recent reports implicate expression of additional members of the GRAS-STAT family in the establishment of nodulation in Medicago truncatula [47, 48]. We note that the flow cytometric method described here should be appropriate for unambiguous determination of the C-value status of root initials responsive to nodulation signals, and of the different cell types that subsequently develop during root nodule formation. If nodule development can be shown to specifically involve G2-arrested cells within the root cortex, this would imply co-option of cellular mechanisms that normally regulate lateral root formation.
In general, the method outlined in this report should be applicable to any transformable plant species within which the regulated expression of HTA6-GFP results in fluorescent nuclei. For promoters of low activity, coupling of nuclear GFP expression to amplification systems (for example provided by GAL4/VP16 ) may be required. Orthologues of histones 2A should be readily accessible for most species, and we have established that a GFP fusion to the rice HTA6 orthologue is targeted to the nucleus in transgenic rice plants (CQZ, C. Santhosh Kumar, V. Sundaresan, and DWG, unpublished results). Plant cell types for which a determination of nuclear DNA content should be of particular interest include those undergoing regulated endoreduplicative cycles, such as found within developing seed storage tissues , within developing trichomes , and in the establishment of symbioses , since the method is not restricted to cells operating within a conventional diploid cell cycle. The method should also be helpful in clarifying reports of the unexpected onset of reductive mitoses within endoreplicated cells . It should also be possible to develop multiparametric flow cytometric methods combining the identification of the C-values of nuclei of specific cell types with a determination of the occurrence of S-phase (relying on antibody-based detection of bromodeoxyuridine incorporation ). This would allow direct determination of the onset of DNA replication particularly within endoreduplicating cells at various C-value levels, thereby providing a greatly increased degree of sophistication in the analysis of processes of this type. The method should also be applicable to lower plants, and could be readily tested using Physcomitrella, which can be transformed and for which the specific G2-arrest within the chloronema has been recently described .
Finally, it should also be noted the flow cytometric method should be equally applicable to transformable non-plant species, including mammals. The relevance of endoreplication to mammalian development, both under normal and abnormal circumstances, is increasingly evident [55, 56], and the ability to accurately chart its occurrence within specific cell types should prove important in the analysis of development as well as of specific disease states.
All general molecular manipulations were done according to standard procedures . PfuUltra™ high-fidelity DNA polymerase (Stratagene, La Jolla, CA, USA) was used for PCR-based amplification of fragments for cloning.
To construct a T-DNA binary vector for expressing GFP in plants, a 2445 bp fragment covering the sGFP expression cassette was released with HincII and SspI from pGFP-JS (Jen Sheen, Massachusetts General Hospital, Boston MA), and inserted into pCAMBIA1302 between the SmaI (9755) and PmlI (752) sites. For convenience of discussion, we call this reassembled vector pCsGFPB. The A. thaliana core histone HTA6 coding sequence (450 bp) was PCR amplified from a cDNA first strand preparation, using forward primer 5'- CATGCCATGGAATCCACCGGAAAAGTG-3' and reverse primer 5'- CATGCCATGGCAGCTTTCTTTGGAGACTTGACTG-3'. The cDNA first strand was prepared using reverse transcriptase SuperScript II according to the manufacturer's recommendations (Invitrogen, Carlsbad, CA, USA). The amplified fragment was inserted into the NcoI site of pCsGFPB. This resulted in in-frame fusion of HTA6 to the N-terminus of GFP, which is downstream of an enhanced CaMV 35S promoter. In the coding region of HTA6, a single nucleotide change at position 118 (G to A) was confirmed by sequencing analysis. This single nucleotide change leads to a point mutation (I39V), and this mutation is retained in all derivative constructs.
Vector pCsGFPB carrying the HTA6 coding sequence was further modified by removing the stop codon (TAA) of the GFP open reading frame as well as the following 14 bp. This modification shifts the contiguous BamHI and XbaI sites to the sGFP open reading frame, and leads to three amino acids (Gly-Ile-Leu) being added to the original sGFP, with the "TAG" within the XbaI site becoming the new stop codon. Then a 70 bp computer generated random sequence (CGAATGTAGTACGTATTCTCCGAACTGAAGCACCTGAGACGTGTAATGTCGGGCCATCTCATACGTACGG) was inserted immediately after the new stop codon, to serve as a transcriptional tag for monitoring the sGFP mRNA level using microarrays printed with the appropriate complementary sequence. Finally, the CaMV 35S promoter (780 bp) upstream of sGFP was excised using EcoRI; and an attR cassette (Frame C, Invitrogen, Carlsbad, CA, USA) was installed. This Gateway-adapted vector was named pCGTAG, and it was used in making the remaining constructs in this study.
Genomic sequences immediately upstream of the start codons of the SCARECROW (SCR), Sulphate Transporter 2-1 (Sultr2-1), SHORTROOT (SHR), and RPL16B coding sequences were PCR amplified. A 2131 bp fragment for SCR was amplified with forward primer 5' CACCGGATAAGGGATAGAGGAAGAGG 3' and reverse primer 5' GGAGATTGAAGGGTTGTTGGTCG 3'. A 2048 bp fragment for Sultr2-1 was amplified with forward primer 5' CACCGCTGACAACTAACACTCCTC-3' and reverse primer 5' CTTCTTCTCGAGTTTTGACGTTGTG 3'. A 2495 bp fragment for SHR was amplified with forward primer 5' CACCGGACAAAGAAGCAGAGCGTGG 3' and reverse primer 5' TTAATGAATAAGAAAATGAATAGAAGAAAGGGAGACCCAC 3'. A 1074 bp fragment for RPL16B was amplified with forward primer 5' CACCTTTCCCACCTCTCTTCAACTTC 3' and reverse primer 5' CGTAAATAGTAAGTTAAATCCCCAAAACGAGGAACG 3'. The five fragments were then cloned into the Gateway entry vector pENTR/D-TOPO (Invitrogen, Carlsbad, CA, USA). The plasmids carrying the regulatory sequences of SCR, Sultr2-1, SHR, and RPL16B were linearized with restriction enzymes EcoRV, EcoRV, EcoNI, DrdI, and EcoRV respectively. These linearized plasmids were employed in the Gateway LR reaction, to insert the individual regulatory sequences into the Gateway-adapted T-DNA binary vector pCGTAG.
Plasmids carrying the above constructs were introduced into Agrobacterium tumefaciens strain GV3101. A. thaliana 'Columbia' (Col-0) was transformed using the floral dip method . Seeds (T1) were harvested and selected on MS agar plates supplemented with 40 mg L-1 hygromycin and 75 mg L-1 carbenicillin. Roots from hygromycin-resistant seedlings were examined for GFP fluorescence using confocal microscopy. Confirmed transformants were transferred to soil.
Introduction of pSCR-HTA6-GFP into plants carrying supernumerary endodermal cell layers
Transgenic A. thaliana seeds carrying SCRpro::SHR were kindly provided by Philip Benfey (Department of Biology, Duke University). The roots of this transgenic line have an increased number of cell layers which display characteristics of the endodermis . We crossed this transgenic line with transgenic plants carrying pSCR-HTA6-GFP. F1 seeds were germinated on MS plates lacking antibiotics. Roots of three-week old seedlings were subjected to confocal and biparametric flow analyses.
Roots from T1 or T2 seedlings were counterstained with 1 μg ml-1 propidium iodide, PI (Sigma, St Louis, MO, USA) for 1 to 2 minutes, and were placed on slides carrying a drop of water for observation. GFP fluorescence was imaged by confocal microscopy using a MRC 1024 MP (Bio-Rad, Hercules CA) confocal scanner attached to an Olympus BX-50 upright microscope, equipped with UPlanFl 4X/0.13, UPlanFl 10X/0.30, and UPlanApo 20X/0.70 objective lenses. LaserSharp2000 (Bio-Rad) was employed for image acquisition and Photoshop 5.0 (Adobe Systems Inc., San Jose, CA) for image processing.
Seeds of Col-0 and of a homozygous transgenic line carrying CaMV35S-HTA6-GFP were sterilized and planted on MS agar plates (2% sucrose, 1.2% agar). The plates were kept at 4°C for three days before transfer to a Conviron growth chamber under 16 hour days / 8 hour nights, with an incident light flux of 150-175 μmol m-2 sec-1, and temperatures of 22°C (day) and 20°C (night). The plates were placed vertically for 3 days. Seedlings of similar sizes were then transferred onto fresh plates, each plate containing ten wild-type and ten transgenic seedlings. The position of the root tip of each seedling was marked on the bottom lid of the plate using a marker pen. Root elongation was measured five days after transfer, and the seedlings were then collected for measurement of fresh weights.
Flow cytometry was done using a MoFlo flow cytometer (Dako Cytomation, Fort Collins, CO) equipped with a Coherent Enterprise II laser providing separate beam paths comprising 50 mW at 365 nm and 200 mW at 488 nm. Homogenates of A. thaliana roots were prepared by chopping , and nuclei were stained by addition of 2 μg/mL 4',6-diamidino-2-phenylindole (DAPI). Samples were analyzed at an event rate of 200 nuclei/s. GFP fluorescence, excited by the 488 nm beam, was detected following reflection by a 555DCLP dichroic beam splitter through a 530/40 band pass filter. DAPI fluorescence, excited by the 365 nm beam, was routed directly through a 450/65 band pass filter. Biparametric histograms of log DAPI versus log GFP signals were triggered on side scatter and collected to a total count of at least 100,000 events.
This work was supported by a grant to DWG from the Plant Genome Program of the National Science Foundation (grant DBI 0211857).
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