@misc{oai:ir.soken.ac.jp:00001445, author = {大栁, 一 and オオヤナギ, ハジメ and OHYANAGI, Hajime}, month = {2016-02-17, 2016-02-17}, note = {It is believed that primordial eukaryotes were derived from prokaryotes, acquiring
nucleus. A number of attempts have been made to reveal the early evolution of
eukaryotes, and some hypotheses for the emergence of the early eukaryotes are
proposed so far. However, the evolutionary process of early eukaryotes is still a
controversial issue and remains one of the biggest questions in current biology. In this
study, with the eventual goal toward elucidation of the evolutionary origin and process
of early eukaryotes, I conducted molecular evolutionary analyses of transporter proteins
of ribosomes between the nucleus and the cytoplasm, called ribosome export factors
(REFs).
 This thesis consists of four chapters and an appendix. In Chapter 1, I described the
research background for this study, with particular emphasis on the molecular function
of the REFs. The ribosome, one of the largest complexes in eukaryotic cells, is to be
exported from the nucleus to the cytoplasm through nuclear pores. As discovered in
recent years, the kinetic steps in this nucleocytoplasmic transport pathway are
stimulated by the REFs. The REFs would be worth focusing on because they can be
considered as one of the components in the eukaryotic core system, translation, and as
one of the key genes in the evolutionary process of early eukaryotes for maintaining the
mobility of the ribosomes under the existence of nuclear membrane in the
then-emerging eukaryotic cells.
 In Chapter 2, with the aim of revealing the functional significance of the REFs in
the process of eukaryotic evolution, I examined the functional constraints of the entire
translation system, the ribosomal proteins and the REF proteins. Estimating the relative
evolutionary rates of the yeast REF proteins, I found that, although not as much as the
ribosomal proteins, the REF proteins do slowly evolve. More interestingly, the
evolutionary rates of the REFs can be classified into two groups. In order to explain this
difference in evolutionary rates between the two groups, I considered two subcategories
for the REFs, according to the steps in which the REFs are involved. Those two
subcategories are non-membranous REFs (non-mREFs) and membranous REFs
(mREFs). Interestingly, this categorization was coincided with the evolutionary rate
difference: Namely, the rapidly evolving REFs were the non-mREFs while the slowly
evolving REFs were the mREFs. These results show that the mREF proteins evolve
slower than the non-mREF proteins, suggesting the functional importance of mREFs in
the evolutionary process of eukaryotes.
 In Chapter 3, I examined the evolutionary origin of the eukaryotic nucleus by
conducting the ortholog detection analysis of the REFs in prokaryotic lineages. The
evolutionary origin of the nucleus is still unclear, although a number of hypotheses have
been proposed so far. I searched for the origin of the REFs in archaeal and eubacterial
lineages by the method of PSI-BLAST. The results obtained showed that the
non-mREFs originated exclusively from eubacterial proteins whereas the mREFs were
from both archaeal and eubacterial proteins. Thus, the REFs working inside the nuclear
membrane (i.e.non-mREFs) are derived only from eubacteria, while alternatively, the
REFs shuttling between the nucleus and the cytoplasm (i.e. mREFs) are from both
archaea and eubacteria. If we assume that the early nucleus has parsimoniously
employed intranuclear proteins as the intranuclear transporters (i.e. non-mREFs), these
data suggest that the structure of the nucleus may be a descendant of the eubacterial cell.
At least, it is suggested that the nucleus arose in a cell that contained chromosomes
possessing a substantial fraction of eubacterial genes. Therefore, from the viewpoint of
ribosome transport, it is plausible that the nuclear structure is not originated from
archaea, but from eubacteria.
 Lastly, in Chapter 4,I provided a summary and conclusions for the present study. I
have shown that the REFs evolve slowly, in addition, the mREFs evolve more slowly,
suggesting that the entire eukaryotic translation system is under the functional
constraints, and in particular, that the mREFs are functionally important in the process
of eukaryotic evolution. Moreover, from the prokaryotic origin of the REFs, it is
suggested that the nucleus is rather a descendant of the eubacterial cell, not the archaeal cell.
 In Appendix, I made particular mention to the biological database projects for
eukaryotes, in which I have been involved. Comprehensive annotations of model
eukaryotes and integrated databases for such annotations are becoming more and more important in the current post-genome era. Moreover, such databases are useful for the study of early evolution of eukaryotes that is the main aim of the present study. Such
databases are also invaluable for comprehensive access to the information resources,
and will stimulate the comparative evolutionary genomics. With the eventual goal to
know the early evolution of eukaryotes, here I refer to three eukaryotic database projects
in which I have been involved, the Molecular Database of Hydra Cells, the Rice
Annotation Project Database (RAP-DB)
, and the H-Invitational Database (H-InvDB).
 The Molecular Database of Hydra Cells includes the invaluable data of expression
patterns of cell type-specific genes in Hydra, a member of phylum Cnidaria, which
branched more than 500 million years ago from the main stem leading to all bilaterian
animals. The database framework was developed by myself, and it serves a unique
opportunity for graphically browsing more than 100 cell type-specific genes in Hydra.
All of the resources can be accessed through http://hydra.lab.nig.ac.jp/hydra/.
 The RAP-DB is a database for Oryza sativa ssp. Japonica, one of the model
eukaryotes, and has been developed in order to comprehensively house all the
annotations produced by the RAP (Rice Annotation Project), which is internationally
organized with the aim of providing standardized and highly accurate annotations of the
rice genome. The latest version of the RAP-DB contains 3l,439 genes validated by
cDNAs. The RAP-DB has been also developed by myself, and employed in the analyses
within Chapter 2. The RAP-DB is available at http://rapdb.lab.nig.ac.jp/.
 The H-Invitational Database (H-InvDB) was originally developed as an integrated
database of the human transcriptome that was based on extensive annotation of large
sets of full-length cDNA (FLcDNA) clone. I participated in the Annotation Meeting of
Genome Information Integration Project for the further development of the human
genome annotations. Now, the database provides annotation for 175,537 human
transcripts and 120,558 human mRNAs extracted from the public DNA databank, in
addition to 54,978 human FLcDNA, in the latest release, H-InvDB_4.3. The H-InvDB
is available at http://www.h-invitational jp/.
 The three projects in which I have been involved produced comprehensive
information for the model eukaryotes. Each database provides a nice implementation for
each biological resource and will stimulate the further exploration in the early evolution
of eukaryotes., application/pdf, 総研大乙第191号}, title = {The early evolution of eukaryotes with special reference to ribosome export factors}, year = {} }