Nucleus The defining feature of eukaryotes is that
their cells have a well-defined, membrane-bound
nucleus, distinguishing them from
prokaryotes that lack such a structure. Eukaryotic cells have a variety of internal membrane-bound structures, called
organelles, and a
cytoskeleton which defines the cell's organization and shape. The nucleus stores the cell's
DNA, which is divided into linear bundles called
chromosomes; these are separated into two matching sets by a
microtubular spindle during nuclear division, in the distinctively eukaryotic process of
mitosis.
Biochemistry Eukaryotes differ from prokaryotes in multiple ways, with unique biochemical pathways such as
sterane synthesis.
Internal membranes Eukaryote cells include a variety of membrane-bound structures, together forming the endomembrane system. Simple compartments, called
vesicles and
vacuoles, can form by budding off other membranes. Many cells ingest food and other materials through a process of
endocytosis, where the outer membrane
invaginates and then pinches off to form a vesicle. Some cell products can leave in a vesicle through
exocytosis. The nucleus is surrounded by a double membrane known as the
nuclear envelope, with
nuclear pores that allow material to move in and out. Various tube- and sheet-like extensions of the nuclear membrane form the
endoplasmic reticulum, which is involved in
protein transport and maturation. It includes the rough endoplasmic reticulum, covered in
ribosomes which synthesize proteins; these enter the interior space or lumen. Subsequently, they generally enter vesicles, which bud off from the smooth endoplasmic reticulum. In most eukaryotes, these protein-carrying vesicles are released and their contents further modified in stacks of flattened vesicles (
cisternae), the
Golgi apparatus. Vesicles may be specialized; for instance,
lysosomes contain
digestive enzymes that break down
biomolecules in the cytoplasm.
Mitochondria somewhat resemble prokaryotic cells. Mitochondria are organelles in eukaryotic cells. The mitochondrion is commonly called "the powerhouse of the cell", for its function providing energy by oxidizing sugars or fats to produce the energy-storing molecule
ATP. Mitochondria have two surrounding
membranes, each a
phospholipid bilayer, the
inner of which is folded into invaginations called
cristae where
aerobic respiration takes place. Mitochondria contain
their own DNA, which has close structural similarities to
bacterial DNA, from which it originated, and which encodes
rRNA and
tRNA genes that produce RNA which is closer in structure to bacterial RNA than to eukaryote RNA. Some eukaryotes, such as the
metamonads
Giardia and
Trichomonas, and the amoebozoan
Pelomyxa, appear to lack mitochondria, but all contain mitochondrion-derived organelles, like
hydrogenosomes or
mitosomes, having lost their mitochondria secondarily. It is thought that mitochondria developed from
prokaryotic cells which became
endosymbionts living inside eukaryotes.
Plastids , which contains
chlorophyll and produces organic compounds by
photosynthesis. Plants and various groups of
algae have plastids as well as mitochondria. Plastids, like mitochondria, have
their own DNA and are developed from
endosymbionts, in this case
cyanobacteria. They usually take the form of
chloroplasts which, like cyanobacteria, contain
chlorophyll and produce organic compounds (such as
glucose) through
photosynthesis. Others are involved in storing food. Although plastids probably had a single origin, not all plastid-containing groups are closely related. Instead, some eukaryotes have obtained them from other eukaryotes through
secondary endosymbiosis or ingestion. The capture and sequestering of photosynthetic cells and chloroplasts,
kleptoplasty, occurs in many types of modern eukaryotic organisms.
Cytoskeletal structures are shown in red,
microtubules in green. (The nucleus is in blue.) The cytoskeleton provides stiffening structure and points of attachment for motor structures that enable the cell to move, change shape, or transport materials. The motor structures are
microfilaments of
actin and
actin-binding proteins. These include α-
actinin,
fimbrin, and
filamin in submembranous
cortical layers and bundles.
Motor proteins of microtubules,
dynein and
kinesin, and
myosin of actin filaments, make the network dynamic. Many eukaryotes have long slender motile cytoplasmic projections, called
flagella, or multiple shorter structures called
cilia.
These organelles are variously involved in movement, feeding, and sensation. They are composed mainly of
tubulin, and are entirely distinct from prokaryotic flagella. They are supported by a bundle of
microtubules arising from a
centriole, characteristically arranged as nine doublets surrounding two singlets. Flagella may have hairs (
mastigonemes), as in many
stramenopiles. Their interior is continuous with the cell's
cytoplasm. Centrioles are often present, even in cells and groups that do not have flagella, but
conifers and
flowering plants have neither. They generally occur in groups that give rise to various microtubular roots. These form a primary component of the cytoskeleton, and are often assembled over the course of several cell divisions, with one flagellum retained from the parent and the other derived from it. Centrioles produce the spindle during nuclear division.
Cell wall The cells of plants, algae, fungi and most
chromalveolates, but not animals, are surrounded by a cell wall. This is a layer outside the
cell membrane, providing the cell with structural support, protection, and a filtering mechanism. The cell wall also prevents
over-expansion when water enters the cell. The major
polysaccharides making up the primary cell wall of
land plants are
cellulose,
hemicellulose, and
pectin. The cellulose
microfibrils are linked together with hemicellulose, embedded in a pectin matrix. The most common hemicellulose in the primary cell wall is
xyloglucan.
Sexual reproduction requires a
life cycle that alternates between a
haploid phase, with one copy of each
chromosome in the cell, and a
diploid phase, with two copies. In eukaryotes, haploid
gametes are produced by
meiosis; two gametes fuse to form a diploid
zygote. Eukaryotes have a life cycle that involves
sexual reproduction, alternating between a
haploid phase, where only one copy of each chromosome is present in each cell, and a
diploid phase, with two copies of each chromosome in each cell. The diploid phase is formed by fusion of two haploid gametes, such as
eggs and
spermatozoa, to form a
zygote; this may grow into a body, with its cells dividing by
mitosis, and at some stage produce haploid gametes through
meiosis, a division that reduces the number of chromosomes and creates
genetic variability. There is considerable variation in this pattern. Plants have both
haploid and diploid multicellular phases. Eukaryotes have lower metabolic rates and longer generation times than prokaryotes, because they are larger and therefore have a smaller surface area to volume ratio. The
evolution of sexual reproduction may be a primordial characteristic of eukaryotes. Based on a phylogenetic analysis, Dacks and
Roger have proposed that facultative sex was present in the group's common ancestor. A core set of genes that function in meiosis is present in both
Trichomonas vaginalis and
Giardia intestinalis, two organisms previously thought to be asexual. Since these two species are descendants of lineages that diverged early from the eukaryotic evolutionary tree, core meiotic genes, and hence sex, were likely present in the common ancestor of eukaryotes. Amoebae, previously regarded as asexual, may be anciently sexual; while present-day asexual groups could have arisen recently. == Evolution ==