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This meant that symbiotic cells contained transcripts produced by both partners (G. elata and M. dendrobii).
Symbiotic cells originate from progenitor cells in the meristem.
These results indicate the formation of differentiated symbiotic cells and confirm the histological analysis.
In zone III, the symbiotic cells are mature and fix nitrogen.
The formation of large symbiotic cells is driven by endoreduplication [4], [5].
The differentiation of symbiotic cells and of bacteroids may therefore constitute signals for the execution of these transcriptome-switches.
Older nodules also may have a root proximal senescence zone (zone IV) composed of degenerating symbiotic cells [3].
In contrast, the bacteria in the symbiotic cells of the second type of mutant nodule were not elongated (Figure 1C).
In the third category, represented by S. meliloti bacA, infected symbiotic cells are formed but bacteria in the symbiosomes fail to differentiate.
The highly endoreduplicated nuclei with DNA contents of 16C, 32C and 64C originate from differentiating or mature symbiotic cells [4], [5], [25].
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Most cDNA libraries have been constructed from non-symbiotic cells and only limited EST datasets were generated.
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