Exam 5 - Remaining Flashcards

(25 cards)

1
Q

Eukaryotic Gene Regulation Compared to Prokaryotic

A

Greater amount of DNA that is associated with histones and other proteins

mRNAs must be spliced, capped, and polyadenylated prior to transport from nucleus

Genes on numerous chromosomes are enclosed in a double membrane nucleus

mRNAs have wide range of half-lives

Modulation of mRNA translation, protein processing, modification, and degradation

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2
Q

Core Promoter Structure in Eukaryotes

A

Comprised of:
-Initiator (Inr)
-TATA-box
-TFiiB recognition element (BRE)
-Downstream promotor element (DPE)
-Motif ten element (MTE)

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3
Q

Function of MTIIA protein

A

Protein that binds to heavy metals and protects cells from toxic effects
Protects cells from oxidative stress
Expressed in low levels in all cells
Transcribed at high levels when exposed to heavy metals

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4
Q

Transcriptional Regulation of MTIIA

A

–Transcription regulatory proteins
–Target cis-acting sites of genes regulating expression
–Activators increase transcription initiation
–Repressors decrease transcription initiation

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5
Q

Basal transcription regulated by:

A

TFIID (and other basal transcription factors)

SP1 – binds at proximal-promoter element GC (contains G-C base pairing)

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6
Q

Modulation of transcription by TF binding to enhancers

A

AP1, AP2, AP4 – regulated by external growth signals

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7
Q

High levels of MTIIA transcription stimulated by

A

Heavy-metal toxicity (MTF-1): Heavy metals bind to MTF-1 and induces a conformation change to allow TF function

Stress (glucocorticoid receptor): Stress causes vertebrates to secrete glucocorticoid
Glucocorticoid binds receptor and induces a conformation change to allow TF function

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8
Q

Transcription repressed by:

A

PZ120 – binds over transcriptional start site

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9
Q

epigenetic trait

A

a stable, mitotically and meiotically heritable phenotype that results from changes in gene expression without alterations in the D N A sequence

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10
Q

Epigenetics

A

the study of the ways in which these changes alter cell- and tissue-specific patterns of gene expression

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11
Q

epigenome

A

refers to the epigenetic state of a cell

During its life span, an organism has one genome, but this genome can be modified in diverse cell types at different times to produce many epigenomes

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12
Q

Epigenetics has been implicated in:

A

Progressive restriction of gene expression during development

Allele-specific expression in gene imprinting

Environment genome interactions during prenatal development that affect adult phenotypes

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13
Q

Monoallelic expression (MAE)

A

Only one allele is transcribed, while the other allele is transcriptionally silent

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14
Q

There are three major classes of MAE

A

Parent-of-Origin Monoallelic Expression: Imprinting

Random Monoallelic Expression: Inactivation of the X Chromosome

Random Monoallelic Expression of Autosomal Genes

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15
Q

Igf2 Imprinting

A

Different expressions based on what you get from chromosomes from each parent. Both parents have the genes but only one gets expressed

Established in the sperm and the egg prior to fertilization.

You only express IGF2 from your dad and H19 from your mom based on methylation

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16
Q

imprinting is an epigenetic process that can be divided into three stages

A

1)Establishment of the imprint during gametogenesis
2) Maintenance of the imprint during embryogenesis and in the adult somatic cells
3) Erasure and reestablishment of the imprint in the germ cells

Thus genomic imprinting is permanent in the somatic cells of an animal

17
Q

Reprogramming in parental germ line

A

Reprogramming occurs in the parental germ line and in the developing embryo just before implantation

After implantation, differential genomic remethylation recalibrates which maternal and paternal alleles will be inactivated

18
Q

Beckwith–Weidemann syndrome

A

Caused by abnormal patterns of DNA methylation resulting in altered patterns of gene expression

19
Q

Prader-Willi syndrome (PWS)

A

Reduced motor function
Obesity
Small hands and feet

Involves a small deletion in chromosome 15 from the father

20
Q

Angelman syndrome (AS)

A

Hyperactivity and thinness
Unusual seizures
Repetitive symmetrical muscle movements
Mental deficiencies

Involves a small deletion in chromosome 15 from the mother

21
Q

Epigenetics and Random Inactivation of the X Chromosome

A

About half of embryonic cells randomly inactivate the maternal X chromosome and the other half inactivate the paternal X chromosome

Effectively silencing almost all the 900 or so genes on whichever homolog is inactivated

Once inactivated, the same X chromosome remains silenced in all cells descended from this progenitor cell

Xic region of the X chromosome: Xist and Tsix

22
Q

Assisted Reproductive Technologies (ART)

A

Imprinted genes play major roles in controlling growth during embryonic and prenatal development

External or internal factors that disturb the epigenetic pattern of imprinting or the expression of imprinted genes can have serious phenotypic consequences

In vitro fertilization (IVF) in humans can cause problems with imprinted genes

23
Q

Environmental Induction of Epigenetic Change

A

Environmental agents including nutrition, chemicals, and physical factors such as temperature can alter gene expression by affecting the epigenetic state of the genome

24
Q

Epigenetics and Diet in Mice

A

The Agouti gene in mice promotes the synthesis of yellow fur pigment; this is called the Avy allele.

Strains of mice carrying the Avy allele show a range of coat colors, from yellow to pseudo-agouti

When pregnant mice were fed a diet that contained chemicals that tend to increase DNA methylation, the offspring tended to have darker fur due to DNA methylation of the Agouti gene

25
Stress-Induced Behavior is Heritable
High maternal mice mothers had increased serotonin which increased histone acylation and decreased DNA methylation. Less stressed phenotype which carried onto offspring. Low maternal mice mothers had decreased serotonin which decreased histone acylation and increased DNA methylation. More stressed phenotype which carried onto offspring.