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In this diagram of a duplicated chromosome, (2) identifies the centromere—the region that joins the two sister chromatids, or each half of the chromosome. In prophase of mitosis, specialized regions on centromeres called kinetochores attach chromosomes to spindle fibers. The centromere links a pair of sister chromatids together during cell ...
Duplicated chromosome. (2) identifies the Monocentric centromere—the region that joins the two sister chromatids, or each half of the chromosome.In prophase of mitosis, specialized regions on centromeres called kinetochores attach chromosomes to spindle fibers.
A karyogram or idiogram is a graphical depiction of a karyotype, wherein chromosomes are generally organized in pairs, ordered by size and position of centromere for chromosomes of the same size. Karyotyping generally combines light microscopy and photography in the metaphase of the cell cycle , and results in a photomicrographic (or simply ...
The sister chromatids will be distributed to each daughter cell at the end of the cell division. Whereas if the chromosome is isobrachial (centromere at centre and arms of equal length), the p and q system is meaningless. At either end of a chromosome is a telomere, a cap of DNA that protects the rest of the chromosome from damage.
Parts of a typical chromosome: (1) Chromatid (2) Centromere (3) Short (p) arm (4) Long (q) arm. In genetics, a locus (pl.: loci) is a specific, fixed position on a chromosome where a particular gene or genetic marker is located. [1]
However, the emergence of research in neocentromeres troubles this conventional definition and questions the function of a centromere beyond being a “landing pad” for kinetochore formation. [4] This expands the scope of the centromere's function to include regulating the function of the kinetochore and the mitotic spindle .
However, due to a lack of full centromere assemblies, base-level understanding of satellite array variation and evolution has remained weak. [5] For example, minisatellite DNA is a short region (1-5 kb) of repeating elements with length >9 nucleotides.
It is formed through the fusion of two chromosome segments, each with a centromere, resulting in the loss of acentric fragments (lacking a centromere) and the formation of dicentric fragments. [1] The formation of dicentric chromosomes has been attributed to genetic processes, such as Robertsonian translocation [1] and paracentric inversion. [2]