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Is the process of nuclear cell division. It is the process of chromosome segregation and nuclear division that follows replication of the genetic material in eukaryotic cells. This process assures that each daughter nucleus receives a complete copy of the organism's genome.
During division, the nucleus of the cell divides, resulting in two sets of identical chromosomes, or organized DNA proteins. This process is almost always accompanied by a process called cytokinesis, in which the rest of the cell divides, leading to two completely separate cells, called daughter cells.
Stages of Mitosis:
Chromosomes are in the dyad form before mitosis, and in the monad form after mitosis.
Prophase: --chromosomes condense --centrioles move to opposite ends of the cell --spindle forms --nuclear envelope disappears
Metaphase: --chromosomes are lined up on cell equator, attached to the spindle at the centromeres
Anaphase: --centromeres divide. Now chromosomes are monads --the monad chromosomes are pulled to opposite poles by the spindle.
Telophase: --chromosomes de-condense --nuclear envelope re-forms --spindle vanishes --cytoplasm divided into 2 separate cells
Sexual reproduction occurs only in eukaryotes. During the formation of gametes, the number of chromosomes is reduced by half, and returned to the full amount when the two gametes fuse during fertilization. For comparison purposes, mitosis is the process of cell division in eukaryotes, in which the parental chromosome number is conserved in each of the daughter cells, while meiosis is a two-cell-division process in sexually reproducing eukaryotes that results in cells (typically gametes) with one-half the chromosome number of the original parental cell.
It is the form of eukaryotic cell division that produces haploid sex cells or gametes (which contain a single copy of each chromosome) from diploid cells (which contain two copies of each chromosome). The process takes the form of one DNA replication followed by two successive nuclear and cellular divisions (Meiosis I and Meiosis II). As in mitosis, meiosis is preceded by a process of DNA replication that converts each chromosome into two sister chromatids.
WHY???
Without meiosis, there would be no sex because every fusion of gametes would increase the number of chromosomes in the progeny. Sexual reproduction is an important survival strategy.
Before meiosis begins genetic material is duplicated. Followed by first division of meiosis.
Duplicated chromosomes condense and become visible. Spindle forms and synapsis occurs. A mixture of RNA and proteins holds the chromosome pairs together. At this time, the homologs exchange parts.
During leptonema stage the chromosomes appear as long single threads. The centrioles move towards the opposite poles of the cell and a definite type of orientation and polarization of chromosomes towards the centrioles take place.
Homolog pairing initiated during leptotene becomes much more intimate during synapsis as the chromosomes become linked by transverse fibers to form the synaptonemal complex. The SC is responsible for the genetic variation and differentiation of species.
During the zygonema stage the homologous chromosomes pair with one another, gene by gene, over the entire length of the chromosomes. Paired homologous chromosomes.
During the pachynema stage each paired chromosome becomes shorter and thicker than in earlier substages and splits into two sister chromatids except at the region of the centromere.
During diplonema stage, chiasmata appear to move towards the ends of the synapsed chromosomes in the process of terminalization and ultimately to slip off the ends.
During diakinesis, the chromosomes begin to coil and so become shorter and thicker. The nucleolus detaches from the nucleolar organizer and disappears completely The nuclear envelope starts to degenerate and spindle formation is well under the way.
Two daughter cells are formed with each daughter containing only one chromosome of the homologous pair. Cell are divided into two.
Presence of nuclear envelope fragments. Spindle forms and fibers attach to both chromosomes.
Nuclear envelopes assemble around two daughter nuclei. Chromosomes decondense. Spindle disappears. Cytokinesis divides cells.
A chromosome is an organized structure of DNA and protein that is found in cells. It is a single piece of coiled DNA containing many genes, regulatory elements and other nucleotide sequences. Chromosomes also contain DNA-bound proteins, which serve to package the DNA and control its functions. The word ''chromosome'' comes from the Greek (''chroma'', color) and (''soma'', body) due to their property of being very strongly stained by particular dyes.
Chromosomes come in pairs. Normally, each cell in the human body has 23 pairs of chromosomes (46 total chromosomes). Half come from the mother; the other half come from the father. Two of the chromosomes (the X and the Y chromosome) determine if you are born a boy or a girl (your gender). They are called sex chromosomes: Females have 2 X chromosomes. Males have 1 X and 1 Y chromosome.
The mother gives an X chromosome to the child. The father may contribute an X or a Y. It is the chromosome from the father that determines if the baby is a girl or a boy. The remaining chromosomes are called autosomal chromosomes. They are known as chromosome pairs 1 through 22.
Each chromosome has a constriction point called the centromere, which divides the chromosome into two sections, or arms. The short arm of the chromosome is labeled the p arm. The long arm of the chromosome is labeled the q arm. The location of the centromere on each chromosome gives the chromosome its characteristic shape, and can be used to help describe the location of specific genes.
Chromosomes vary widely between different organisms. The DNA molecule may be circular or linear, and can be composed of 10,000 to 1,000,000,000 nucleotides in a long chain. Typically eukaryotic cells (cells with nuclei) have large linear chromosomes and prokaryotic cells (cells without defined nuclei) have smaller circular chromosomes, although there are many exceptions to this rule. Cells may contain more than one type of chromosome; for example, mitochondria in most eukaryotes and chloroplasts in plants have their own small chromosomes.
FUNCTIONS: Cell Division Process Gene Packaging Packaging of Regulatory Elements DNA Packaging
Composed of enormously long circular or linear molecules of DNA. Contains the genetic information that defines each organism- its GENOME.
3 Classes of specialized DNA sequences are needed to make a fully functional chromosome. 1. A Centromere 2. Two Telomeres 3. An origin of DNA replication .
Chromosomal locus that regulates the movements of the chromosomes during mitosis and meiosis. Defined by specific DNA sequences plus proteins that bind to them. The heart <3 of all chromosomal movements in mitosis and meiosis.
Has an important role in monitoring the attachment of the chromosomes to the spindle and controlling the progress of the cells through mitosis. STRUCTURE: waist-like structure or primary constriction where two sister chromatids are most intimately paired.
Protects the ends of the chromosomal DNA molecules and ensure their complete replication.
A. Chromosomes found in Human B. Chromosome can be categorized on the basis of following criteria. 1. Number of centromeres 2. Position of centromeres
Chromosomes are highly dispersed and difficult to locate before cell division. When the cell begins to divide, the chromosomes are seen clearly and can be photographed as well as their morphology, size and shape can be studied. The chromosome types are divided into two categories Autosomes Sex Chromosome.
A. Autosomes
Autosomes are structures that contain the hereditary information. They do not contain information related to reproduction and sex determination. They are identical in both sexes, i.e., male and female species of humans. There are 46 (2n) chromosomes in humans. Of these 46 chromosomes, there are 44 pairs of autosomes and contain information related to the phenotypic characters.
B. Allosomes/ Heterosomes
The allosomes are sex chromosomes that are different from autosomes in form, behavior and size. There are a pair of allosomes in humans. The X chromosomes are present in the ovum and either the X or Y chromosome can be present in the sperm. These chromosomes help in determination of sex of the progeny. If the offspring receives X chromosome from the mother as well as father, it results in a female child (XX). If the offspring receives one X and one Y chromosome from the parents, it results in a male child (XY). In simple words, it is the donation of X or Y chromosome by the father that helps in determination of the sex of the child.
Apart from these two categories, chromosomes can further be divided according:
TO THE LOCATION OF THE CENTROMERE
NUMBER OF CENTROMERES
Acentric Chromosome
Monocentric Chromosome Dicentric Chromosome Polycentric Chromosome
Telocentric Chromosome
Subtelocentric Chromosome Acrocentric Chromosome
Holocentric Chromosome
Chromosomes Diffuse
Holocentric Chromosome In holocentric chromosomes, the centromere runs through the entire length of the chromosome. These chromosomes are very common in cells belonging to organisms in the animal and plant kingdom. In this type of Chromosomes Diffuse the centromere is non-localized. the most well known example being the nematode Caenorhabditis elegans
Found in Human
Autosomes Allosomes (Sex Cells) 1 pair of chromosome
22 pairs of chromosomes
Shape v-shaped
Near centre Two unequal J or L shaped human being (sub-median) arms Near at one end (subterminal) Terminal One arm very short and another long Rod like grasshopper drosophila
Acrocentric Telocentric
Number of centromeres
none One Two
Three Many Diffused (Here, microtubules are attached along the length of chromosome)
References:
For chromosomes: