Unit 1 Flashcards

1
Q

Methyl Groups Effect on Genes

A

Methyl groups (CH3) can attach to DNA, typically at cytosine bases, leading to gene silencing by preventing gene expression.

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2
Q

Epigentic Therapy

A

A treatment approach that aims to alter epigenetic marks (like DNA methylation and histone modification) to correct gene expression patterns in diseases like cancer.

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3
Q

Histones

A

Proteins around which DNA is wrapped. Modifications to histones can change gene accessibility and activity, influencing gene expression.

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4
Q

Types of Epigentic Tags

A

Epigenetic tags include DNA methylation, histone modifications (like acetylation and methylation), and non-coding RNA molecules, all of which regulate gene expression without altering the DNA sequence.

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5
Q

Methylation

A

The addition of a methyl group to DNA or histones, typically leading to gene silencing or reduced gene expression.

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6
Q

Acetylation

A

The addition of acetyl groups to histones, which relaxes the DNA structure, making genes more accessible for transcription and thus increasing gene expression.

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7
Q

Methyl Groups

A

Small chemical groups (CH3) that can attach to DNA or histones and typically repress gene activity by altering chromatin structure.

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8
Q

Acetyl Groups

A

Chemical groups (COCH3) that can be added to histones to loosen DNA wrapping, allowing gene expression to increase.

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9
Q

Epigenome to Active VS Inactive Genes

A

The epigenome refers to chemical changes to DNA and histones that control whether genes are turned on (active) or off (inactive) without changing the underlying DNA sequence.

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10
Q

GR Gene

A

(Glucocorticoid Receptor gene): This gene encodes a receptor for cortisol. Its expression is influenced by epigenetic modifications, affecting stress responses.

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11
Q

GFP Gene Tightly Wound VS Loose

A

(Green Fluorescent Protein) tightly wound vs loose: When GFP gene DNA is tightly wound around histones (heterochromatin), it’s inactive. When loose (euchromatin), the gene is active and can be transcribed.

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12
Q

Epigenome Relation to Protein Synthesis

A

The epigenome influences protein synthesis by regulating gene expression. Modifications to DNA and histones can either promote or inhibit the transcription of genes, ultimately affecting the proteins produced.

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13
Q

Methyl Groups Attatch

A

Upstream of gene promoter

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14
Q

Methyl Groups Effect Transcription

A

Methylation of DNA typically represses gene transcription by making the DNA more compact and inaccessible to the transcription machinery.

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15
Q

Acetyl Groups Effect Gene Expression

A

Acetyl groups are added to histones, causing histones to loosen their grip on DNA. This makes the DNA more accessible and promotes gene expression.

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16
Q

Acetyl Groups Attatch

A

Acetyl groups are added to the lysine residues of histones, leading to a relaxed chromatin structure and increased gene expression.

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17
Q

Histones to Epignetics

A

Histones are proteins around which DNA is wrapped. Modifications to histones (e.g., acetylation, methylation) can influence how tightly or loosely the DNA is wound, affecting gene expression.

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18
Q

Methyl VS. Acetyl on DNA/Histones to Chase Change

A

Methyl groups add to DNA or histones and typically repress gene expression by tightening DNA packaging. Acetyl groups, added to histones, loosen DNA wrapping, making it more accessible for transcription and increasing gene expression.

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19
Q

Acetyl Increase in Relation to mRNA Production

A

Increased acetylation of histones generally leads to increased mRNA production as it makes DNA more accessible for transcription.

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20
Q

Types of Stem Cells

A

The main types of stem cells are embryonic stem cells, adult stem cells, and induced pluripotent stem (iPS) cells.

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21
Q

Embryonic Stem Cells

A

These are pluripotent stem cells derived from the early-stage embryo. They can differentiate into almost any cell type in the body.

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22
Q

Pluripotent

A

Pluripotent cells can differentiate into all cell types of the body, except for extra-embryonic tissues like the placenta.

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23
Q

Adult Stem Cells

A

These are multipotent stem cells found in various tissues in the body. They can differentiate into a limited range of cell types related to the tissue from which they are derived.

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24
Q

Multipotent

A

Multipotent cells can differentiate into a limited number of cell types, typically related to the tissue or organ from which they originate.

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Advantages and Disadvantages of Adult Stem Cells
Advantages: They are less likely to cause immune rejection since they come from the patient’s own body. They are also ethically less controversial than embryonic stem cells. Disadvantages: They are more limited in the types of cells they can become and are harder to isolate in large numbers.
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iPS Cells
These are adult cells that have been reprogrammed to become pluripotent. They can differentiate into nearly any cell type.
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Advantages and Disadvantages of iPS Cells
Advantages: They are less ethically controversial because they don't require embryos, and they can be made from a patient’s own cells, reducing immune rejection. Disadvantages: The reprogramming process can sometimes result in genetic mutations, and the risk of tumor formation is a concern.
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Undifferentiated
Cells that have not yet specialized into a specific cell type. They can develop into various types of cells depending on their environment and signals.
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Potential of Multipotent and Pluripotent Cells
Multipotent cells can differentiate into a limited range of related cell types (e.g., adult stem cells). Pluripotent cells can differentiate into nearly all cell types of the body (e.g., embryonic stem cells, iPS cells).
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Advantages VS Disadvantages of Multipotent and Pluripotent Cells
Multipotent: Advantages: Lower risk of tumor formation, less ethical controversy, and less immune rejection. Disadvantages: Limited in the types of cells they can become. Pluripotent: Advantages: Can become any cell type, offering broader research and therapeutic potential. Disadvantages: Higher risk of tumor formation, ethical concerns, and difficulty in obtaining.
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Levels of Understandings of Multipotent and Pluripotent Cells
Multipotent cells are better understood because they have been studied for longer, particularly in tissue regeneration. Pluripotent cells are still under intense research for their ability to differentiate into almost any cell type, but there are more complexities regarding their safe use and behavior.
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Type of Researcher That Uses Blastocysts
Research on embryonic stem cells, developmental biology, early human development, and regenerative medicine often uses blastocysts.
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Model Organisms Used to Study
Model organisms are used to study genetics, developmental biology, disease mechanisms, drug testing, and physiological processes that are similar to humans or other organisms.
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Commonly Used Model Organisms
Plant: Arabidopsis thaliana Invertebrate: Drosophila melanogaster (fruit fly) Vertebrate: Mus musculus (mouse) Prokaryote: Escherichia coli (bacterium) Eukaryote: Saccharomyces cerevisiae (yeast)
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Characteristics of Planaria That Make Them Ideal Model Organisms
Planaria have remarkable regenerative abilities, allowing them to regrow entire body parts, making them ideal for studying regeneration and stem cell biology.
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Planaria Husbandry
Planaria are kept in clean, aquatic environments with a controlled temperature. They are typically fed small pieces of food like liver or other organic matter.
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Characteristics of Fruit Flies That Make Them Ideal Model Organisms
Fruit flies are small, reproduce quickly, have a well-mapped genome, and are easy to manipulate genetically, making them ideal for genetic research.
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Male VS Female Fruit Fly and Identifying
Males are smaller, have darker coloration on their abdomen, and possess a rounded abdomen. Females are larger, with a more pointed abdomen and a lighter, striped pattern on their abdomen. They also have a broader body compared to males.
39
Transgenic
An organism that has been genetically modified to contain genes from another species, allowing for the expression of new traits.
40
Bioremeditation
The use of living organisms, often microorganisms, to remove or neutralize pollutants from the environment, such as oil spills or contaminated water.
41
Recombinant DNA Technology
A set of techniques used to combine DNA from different sources, creating new genetic combinations that are valuable in medicine, agriculture, and research.
42
Cloning Vector
A small DNA molecule used in genetic engineering to carry foreign DNA into a host cell, allowing the foreign DNA to be replicated or expressed.
43
Plasmid
A small, circular piece of DNA found in bacteria that can carry foreign genes and replicate independently of chromosomal DNA. Plasmids are commonly used as cloning vectors in molecular biology.
44
Examples of Vectors
Plasmids, bacteriophages, yeast artificial chromosomes (YACs), and viral vectors are commonly used to transfer genes into cells.
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Many Body Sections of a Journal Article
Introduction Methods Results Discussion
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Title
Title Authors Address
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Header VS Title
Header has shortened version of title and page numbers
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Address
Below authors Lab experiment took place
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Author Order
Lead author first and principle investigator last
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Abstract
Concise summary of the key points of your research Overview of: Justification Research Topic/Question/ hypothesis Methods Results Data Analysis Conclusions and a List of Key Words at bottom
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Intro
Full, ORGANIZED, overview of your topic and review of the literature. Restate research question Justification of research Background Overview of methods not step by step
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Results
Start with overview What was your assay? Qualitative or quantitative? Do NOT include data of planaria that did not survive. Save for discussion.
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Captioning Photos
describe the image in detail, be in complete sentences, and be referenced in the text. Cite all images not generated by the authors. picture, graph, table
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In Text Citation Paragraphs
Introduction, methods, discussion
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Formatting References
Last name and first/middle initials for all authors up to and including 20 authors. Separate each author’s initials from the next author with a comma. Use an ampersand (&) before the last author’s name. If there are 21 or more authors, use an ellipsis (but no ampersand) after the 19th author, and then add the final author’s name. For multiple articles by the same author, or authors listed in the same order, list the entries in chronological order from earliest to most recent. Year only unless news article Jounral name out fully Italicize title, journal article and volume Group and author become same Lastname, F. M. (Year, Month Date). Title of page. Site name. URL
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Formatting In Text Citations
(Last name, Year) If there is not author use the first part of the reference (organization, year) or (title, year) No Author Initials are included No Month/Day is included And with two authors Three or more authors is followed by et al.
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crapoli
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crapinski
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