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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 ...
The largest regions on each chromosome are the short arm p and the long arm q, separated by a narrow region near the center called the centromere. [1] Other specific regions have also been defined, some of which are similarly found on every chromosome, while others are only present in certain chromosomes. Named regions include: Arms (p and q ...
an inner kinetochore, which is tightly associated with the centromere DNA and assembled in a specialized form of chromatin that persists throughout the cell cycle; an outer kinetochore, which interacts with microtubules ; the outer kinetochore is a very dynamic structure with many identical components, which are assembled and functional only ...
During cell division, the identical copies (called a "sister chromatid pair") are joined at the region called the centromere (2). Once the paired sister chromatids have separated from one another (in the anaphase of mitosis) each is known as a daughter chromosome. The short arm of the right chromatid (3), and the long arm of the right chromatid ...
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.
Centromere protein A, also known as CENPA, is a protein which in humans is encoded by the CENPA gene. [5] CENPA is a histone H3 variant which is the critical factor determining the kinetochore position(s) on each chromosome [ 6 ] in most eukaryotes including humans.
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]