Cell Differentiation and Gene Flashcards
What is the difference between cell differentiation and cell determination?
Cell DIFFERENTIATION is the production of different cell types within an organism.
Cell DETERMINATION is the stability of cell differentiation even after the end of any inducing signal (basically, the memory of differentiation). It is transmitted to the daughter cells.
What is gene expression?
It is the whole process leading to the synthesis of the final product of a given gene, either a protein or a functional RNA.
What is cell modulation?
It is the simple, reversible change in gene expression, but no change in the cell type. |t is also known as adaptation.
What are the differences between cell determination and cell modulation?
Cell differentiation is a STABLE, COMPLEX change, while cell modulation is a TEMPORARY, SIMPLE change.
How do we know that all differentiated cells have a complete genome?
We know this from cloning experiments, an example being Dolly the sheep. A whole differentiated (mammary epithelial) sheep cell was fused to the cytoplasm of a sheep oocyte (egg cell), which resulted in the proliferation of the cell, leading to the birth of Dolly.
Thus we know that the differentiated cell had all the genes necessary (the entire genome).
What is meant by the ‘programme of differentiation’?
It is the diverse set of cell-type-specific genes that are generally activated in expression during one step in lineage, while others are repressed.
What are DNA ‘probes’, and what is their purpose?
They are DNA with a known sequence which is complementary to the sequence you are searching for. This reveals many mRNA differences between any 2 cell types.
What are DNA ‘probes’, and what is their purpose?
They are DNA with a known sequence which is complementary to the sequence you are searching for. This reveals many mRNA differences between any 2 cell types.
What are the two ways in which our bodies control transcription?
Chromatin remodelling/folding and specific transcriptional regulation.
Describe chromatin remodelling/folding.
Our chromatin exists in two forms: euchromatin and heterochromatin. Euchromatin is our active form; the DNA is not compactly stored. Heterochromatin is our inactive form; here, the chromatin is tightly packed, interfering with transcription.
One mechanism of increasing chromatin folding (ie. converting eu- to heterochromatin) is DNA methylation. It occurs on cytosine within a CpG pair, changing it to methylcytosine. It is copied to the opposite strand in replication by a maintenance methyltransferase. This means that the methylation pattern is ‘remembered’ in daughter cells.
Unmethylated pairs can become methylated by de novo methylation, carried out by de novo methyltransferase.
This methylated DNA becomes highly folded.
What is the role of transcription factors in specific transcriptional regulation?
Transcription factors are regulators of transcription. They are proteins that physically fit onto a specific DNA sequence.
They can bind to specific sequences on a gene promoter, and alter transcription of that gene (either increase or decrease).
What are master gene regulators?
They regulate transcription of a whole set of lineage-specific genes (a ‘program’) for a given cell type.
Describe the mechanism of a master gene regulator.
Transcription of the gene for the master gene regulator occurs, creating the regulatory proteins. These proteins then bind to and activate the promoters of different genes coding for proteins that will differentiate the cell. These specialised proteins are made, and then proceed to work on the cell.
What are the three patterns of cell division (ie. how much they divide)?
- cells that are constantly being replaced (eg. in bone marrow, gut epithelium, epidermis)
-cells that divide very little, but can divide more to repair damage (eg. liver cells, endothelium)
-cells that cannot divide, and may not be replaced when lost (eg. neurons, lens)
