THESIS
2014
x, 91 leaves : illustrations ; 30 cm
Abstract
Dinoflagellates are an exceptional group of unicellular microorganisms that exhibit a
novel perspective in chromatin biology as they bear a number of unique characteristics. Their
genome sizes are the largest among eukaryotes. Despite this, the conventional nucleosomal
organization in eukaryotic chromosomes are not detectable in the nucleus of dinoflagellates. A
group of dinoflagellates Histone-Like Proteins (HLPs) are the major nuclear basic proteins.
They were proposed to be the candidate for regulating gene expression and maintaining the
extra-chromosomal loops due to their abundance and localization. Another significant group
of basic nuclear proteins, the Dinoflagellate Viral Nucleoproteins (DVNPs), were recently
suggested to be related to the genome expansion and loss of n...[
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Dinoflagellates are an exceptional group of unicellular microorganisms that exhibit a
novel perspective in chromatin biology as they bear a number of unique characteristics. Their
genome sizes are the largest among eukaryotes. Despite this, the conventional nucleosomal
organization in eukaryotic chromosomes are not detectable in the nucleus of dinoflagellates. A
group of dinoflagellates Histone-Like Proteins (HLPs) are the major nuclear basic proteins.
They were proposed to be the candidate for regulating gene expression and maintaining the
extra-chromosomal loops due to their abundance and localization. Another significant group
of basic nuclear proteins, the Dinoflagellate Viral Nucleoproteins (DVNPs), were recently
suggested to be related to the genome expansion and loss of nucleosomes during the course of
dinoflagellates evolution. The biological functions of this group of protein have yet to be
revealed.
The CcDVNP1 gene was cloned in Crypthecodinium cohnii. This CcDVNP1 from C.
cohnii was shown to exhibit similar molecular properties of those DVNPs from other
dinoflagellates. The transcript and expression level of CcDVNP1 were shown to peak at G2/M
phase during the cell cycle, which followed a similar expression pattern to that of HCc3.
DNA-damage could induce the up-regulation of CcDVNP1, whereas incubation under high
temperature posed no effects on the expression of CcDVNP1. On the other hand, osmolarity
stress could significantly reduce the transcript level of CcDVNP1. Inhibiting the three classes
of RNA polymerases surprisingly increased the protein expression level of CcDVNP1.
Integrating all the experimental data, I proposed that DVNP is involved in the regulation of
transcriptional activities.
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