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The four main steps of meiosis II are: prophase II, metaphase II, anaphase II, and telophase II. In prophase II, we see the disappearance of the nucleoli and the nuclear envelope again as well as the shortening and thickening of the chromatids. Centrosomes move to the polar regions and arrange spindle fibers for the second meiotic division.
Prophase is the first stage of mitosis in animal cells, and the second stage of mitosis in plant cells. [10] At the start of prophase there are two identical copies of each chromosome in the cell due to replication in interphase. These copies are referred to as sister chromatids and are attached by DNA element called the centromere. [11]
Crossing over occurs between prophase I and metaphase I and is the process where two homologous non-sister chromatids pair up with each other and exchange different segments of genetic material to form two recombinant chromosome sister chromatids. It can also happen during mitotic division, [1] which may result in loss of heterozygosity.
Both proper initial segregation of chromosomes in prophase I and the next chromosome segregation during equational division in meiosis II are required to generate gametes with the correct number of chromosomes. CO recombinants are produced by a process involving the formation and resolution of Holliday junction intermediates.
The SC protein scaffold stabilizes the physical pairing of homologous chromosomes by polymerizing between them during meiotic prophase. [2] During synapsis, autosomes are held together by the synaptonemal complex along their whole length, whereas for sex chromosomes , this only takes place at one end of each chromosome.
Three types of cell division: binary fission (taking place in prokaryotes), mitosis and meiosis (taking place in eukaryotes).. When cells are ready to divide, because cell size is big enough or because they receive the appropriate stimulus, [20] they activate the mechanism to enter into the cell cycle, and they duplicate most organelles during S (synthesis) phase, including their centrosome.
The metaphase chromosomes are treated with trypsin (to partially digest the chromosome) and stained with Giemsa stain. Heterochromatic regions, which tend to be rich with adenine and thymine (AT-rich) DNA and relatively gene-poor, stain more darkly in G-banding.
GVBD is the process of nuclear envelope dissolution and chromosome condensation similar to mitotic prophase. In females, the process of folliculogenesis begins during fetal development. Folliculogenesis is the maturation of ovarian follicles. Primordial germ-cells (PGC’S) undergo meiosis leading to the formation of primordial follicles. [6]