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As a consequence of this process, the nuclear genome of most eukaryotes including humans is colonized by NUMTs.
Esterified sterols, a core component of lipid storage particles, represent a major storage of cellular sterols in most eukaryotes, including yeast [31], [32].
Establishment of the Oxa1 and Oxa2 subfamilies appears to have occurred following an ancient duplication, because most eukaryotes, including plants and opisthokonts possess two Oxa genes [70].
In most eukaryotes including humans, this process is catalyzed by Dmc1 and Rad51 proteins, which are structural and functional homologues of bacterial and archaeal recombinases, RecA and RadA [3], [9], [10].
Cell polarity is determined by the structure of the actin cytoskeleton in most eukaryotes, including yeast.
Most eukaryotes, including plants, have only a small number of E1 enzymes and multiple E2 and E3 enzymes.
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Conversely, most unicellular eukaryotes, including the green alga Chlamydomonas reinhardtii, have typical cilia and well conserved IFT genes but lack RFX TFs.
In budding yeast, only a small number (3.8%) of genes have introns [ 24], whereas in most other eukaryotes, including Drosophila, intronic sequences are a feature of the majority of genes and must be excised to produce a functional mRNA [ 25].
P. infestans contains a large kinome compared to that of most other lower eukaryotes, including fungal plant pathogens that occupy similar environmental niches but typically express only about 100 ePKs and less than 10 aPKs [ 54].
Because sequence homology among Scc3 orthologs stretches throughout the entire Z. rouxii structure (Fig. 1-fig.sup.3), most if not all features are likely to be shared by orthologs from a wide variety of eukaryotes including most animals, plants, and protozoa.
Although, the mitochondria of many other eukaryotes, including most plants, use the standard code.
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