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Epigenetics
1. What is epigenetics
2. Discuss its functions and consequences
3. Discuss how epigenetics affects humans and microorganisms
I. Epigenetics
Epigenetics is the study of heritable changes in gene activity that are not caused by changes
in the DNA sequence; it also can be used to describe the study of stable, long-term alterations in
the transcriptional potential of a cell that are not necessarily heritable. Unlike simple genetics
based on changes to the DNA sequence (the genotype), the changes in gene expression or
cellular phenotype of epigenetics have other causes
Epigenetics involves genetic control by factors other than an individual's DNA sequence.
Epigenetic changes can switch genes on or off and determine which proteins are transcribed.
Epigenetics is involved in many normal cellular processes. Consider the fact that our cells all
have the same DNA, but our bodies contain many different types of cells: neurons, liver cells,
pancreatic cells, inflammatory cells, and others. How can this be? In short, cells, tissues, and
organs differ because they have certain sets of genes that are "turned on" or expressed, as well as
other sets that are "turned off" or inhibited. Epigenetic silencing is one way to turn genes off, and
it can contribute to differential expression. Silencing might also explain, in part, why genetic
twins are not phenotypically identical. In addition, epigenetics is important for X-chromosome
inactivation in female mammals, which is necessary so that females do not have twice the
number of X-chromosome gene products as males. Thus, the significance of turning genes off
via epigenetic changes is readily apparent.
The term also refers to the changes themselves: functionally relevant changes to the genome
that do not involve a change in the nucleotide sequence. Examples of mechanisms that produce
such changes are DNA methylation and histone modification, each of which alters how genes are
expressed without altering the underlying DNA sequence. Gene expression can be controlled
through the action of repressor proteins that attach to silencer regions of the DNA. These
epigenetic changes may last through cell divisions for the duration of the cell's life, and may also
last for multiple generations even though they do not involve changes in the underlying DNA
sequence of the organism; instead, non-genetic factors cause the organism's genes to behave
differently.
II. Functions and Consequences
Somatic epigenetic inheritance through epigenetic modifications, particularly through DNA
methylation and chromatin remodeling, is very important in the development of multicellular
eukaryotic organisms. The genome sequence is static (with some notable exceptions), but cells
differentiate into many different types, which perform different functions, and respond
differently to the environment and intercellular signalling. Thus, as individuals develop,
morphogens activate or silence genes in an epigenetically heritable fashion, giving cells a
"memory". In mammals, most cells terminally differentiate, with only stem cells retaining the
ability to differentiate into several cell types ("totipotency" and "multipotency"). In mammals,
some stem cells continue producing new differentiated cells throughout life, such as in
neurogenesis, but mammals are not able to respond to loss of some tissues, for example, the
inability to regenerate limbs, which some other animals are capable of. Unlike animals, plant
cells do not terminally differentiate, remaining totipotent with the ability to give rise to a new
individual plant. While plants do utilise many of the same epigenetic mechanisms as animals,
such as chromatin remodeling, it has been hypothesised that some kinds of plant cells do not use
or require "cellular memories", resetting their gene expression patterns using positional
information from the environment and surrounding cells to determine their fate.
In medicine, Epigenetics has many and varied potential medical applications as it tends to be
multidimensional in nature.[81] Congenital genetic disease is well understood, and it is also clear
that epigenetics can play a role, for example, in the case of Angelman syndrome and Prader-Willi
syndrome. These are normal genetic diseases caused by gene deletions or inactivation of the
genes, but are unusually common because individuals are essentially hemizygous because of
genomic imprinting, and therefore a single gene knock out is sufficient to cause the disease,
where most cases would require both copies to be knocked out.
Sources:
http://en.wikipedia.org/wiki/Epigenetics#Epigenetics_in_microorganisms
http://hmg.oxfordjournals.org/content/16/R1/R28.full http://epigenie.com/epigenetics/