What does CEN mean in BRITISH MEDICINE


CEN (also known as Centromere) is an abbreviation used to refer to a specialized DNA sequence found in the genome of most organisms. This central region of a chromosome holds two sister chromatids together, and is essential for the separation of chromosomes during cell division. It is also the site where spindle fibers attach during mitosis and meiosis. CEN stands for centromere, which has an important role in chromosomal movement and segregation. In humans, it can be located anywhere on the chromosome, although it may sometimes be difficult to identify and locate in certain species.

CEN

CEN meaning in British Medicine in Medical

CEN mostly used in an acronym British Medicine in Category Medical that means centromere

Shorthand: CEN,
Full Form: centromere

For more information of "centromere", see the section below.

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Definition

A centromere is a specific sequence of DNA located at the center of each chromosome. CEN molecules are generally present on all chromosomes and are extremely critical for dividing chromosomes correctly during cell division. Without CEN molecules, cells would not be able to divide properly or form normal copies of themselves during mitosis or meiosis. As a result, mutations that disrupt the location or function of CEN proteins can cause severe genetic diseases such as leukemia or Down’s Syndrome.

Function

The centromere plays an important role in facilitating accurate chromosome segregation during both mitosis and meiosis. In cells undergoing mitotic divisions (division into two daughter cells with identical genetic material), the centromere helps organize sister chromatids by attaching them together with cohesin proteins so that they do not separate prematurely from one another before entering into telophase/cytokinesis stage at which they are normally split apart into daughter cells. During meiotic divisions (the process of producing haploid gamete cells through genetic recombination), spindle fibers attach themselves to the centromeres so that homologous chromosomes segregate correctly while crossing over takes place between non-sister chromatids.

Role in Disease

Mutations affecting centromeres can have significant health implications since they can interfere with proper chromosome separation resulting in aneuploidy (chromosome number abnormalities). Mutations occurring on either side or within a centromere can lead to mispairing and missegregation when crossing over occurs during meiosis, which results in increased frequency of numerical chromosome disorders such as trisomy 21 (Down's Syndrome). Abnormalities in gene dosage caused by mutations disrupting either structure or function of centromeres has also been linked to certain types of cancer including lymphoma.

Essential Questions and Answers on centromere in "MEDICAL»BRITMEDICAL"

What is a Centromere?

A centromere is a region of the chromosome that binds two chromatids together. It is located in the middle of the chromosome, and its primary role is to maintain the structural stability of the chromosome during cell division.

How does a Centromere work?

During cell division, the centromere ensures that each daughter cell receives one complete set of chromosomes by binding sister chromatids together. Without it, chromosomes would become fragmented and cause genetic disorders.

What are Sister Chromatids?

Sister chromatids are identical copies of each other formed by DNA replication prior to cell division. They remain attached to each other at the centromere until they separate in anaphase to form two new daughter cells.

Is there more than one type of Centromere?

Yes, there are three types of centromeres; point, regional (or diffuse), and satellite. Point centromeres contain only alpha satellites which are short stretches of DNA repeated many times throughout a genome; regional or diffuse centromeres contain multiple types of repeats; and satellite centromeres contain large arrays of long repeating units such as microsatellites or minisatellites.

What happens when a Centromere malfunctions?

When a centromere malfunctions due to either environmental or genetic factors, it can cause serious chromosomal instability which can result in diseases such as Down Syndrome or birth defects such as spina bifida. These conditions can be devastating and therefore it is important for medical professionals to be aware of any potential issues related to the functioning of the centromere.

How do scientists study Centromeres?

Scientists use various techniques such as immunofluorescence microscopy, FISH (Fluorescent In Situ Hybridization), and molecular cloning in order to study how these structures function and their involvement in cellular processes like meiosis/mitosis and gene expression.

Could mutations in Centromeres be used for gene-editing?

Yes! Mutations that occur at certain regions on the structure can be used for targeted gene editing using methods like CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats). This has been explored for potential applications in creating better crops, mitochondrial diseases treatments, alternative forms breast cancer therapies, etc.

Does every organism have Centromeres?

Not necessarily! While all eukaryotic organisms possess them - organisms whose cells possess a nucleus - not all prokaryotes do - those whose cells don't possess a nucleus - instead possessing proteins referred to as plasmid origins which serve similar roles by enclosing loops within their cellular walls during replication/division operations. However, more research needs to be done before we have an exact understanding about how these functions behave within prokaryotes.

Are Centromeres evolutionary conserved?

Yes! The same features that define our human chromosomes can also found throughout different species from fungi even plants suggesting they have remained resilient throughout hundreds millions years evolution.

Final Words:
In conclusion, CEN stands for Centromere which is an essential component within chromosomes providing structural stability and ensuring correct heredity during cell division through attachment sites enabling sister chromatid cohesion and spindle fiber attachment respectively. Most importantly, proper functioning and expression levels of CEN molecules play a crucial role in preventing chromosomal disorders caused by faulty meiotic segregation during cell division."

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