Final Exam Flashcards

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1
Q

Mutant screen

A

a process where researchers examine a large number of mutagenized organisms and identify rare individuals with a mutant phenotype of interest

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2
Q

What is the last photoreceptor cell to be assembled into the ommatidia of the Drosophila eyes?

A

R7 photoreceptor cell

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3
Q

What is the function of R7 photoreceptor cells?

A

Contains rhodopsin proteins that enable flies to detect UV light

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4
Q

Why do you separate mutations into groups?

A

You want to determine the number of different mutant genes represented in a collection which is achieved by sorting the mutations into complementation groups, each containing different mutant alleles of the same gene

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5
Q

What are two methods in which scientists verify gene assignment to prevent wrong gene identification?

A

1) Add back a transgenic copy of the wild-type presumptive gene to the mutant organisms, to see if a wild-type phenotype results
2) TALENs–> mutagenize the candidate gene in an otherwise wild-type organisms to establish whether the mutant phenotype is produced

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6
Q

What is the function of the Sev gene?

A

A transmembrane receptor protein present on the surface of R7 precursor cells

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7
Q

What is the function of the Boss gene?

A

transmembrane ligand present on the R8 surface

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8
Q

What happens when R7 contacts R8; Boss binds Sev?

A

A signal transduction cascade is initiated within the R7 precursor cell resulting in expression of genes that determine R7 cell fate

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9
Q

pleiotropic

A

genes that are required for more than one developmental pathway

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10
Q

redundant genes

A

genes whose products serve the same function in a pathway

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11
Q

How do scientists try to identify pleiotropic genes in a developmental pathway?

A

Modifier screen

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12
Q

Mutations that cause the eyes of sev hypomorphs to appear more mutant

A

dominant enhancers (E-)

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13
Q

Mutations that cause sev hypomorphic eyes to appear more like wild-type

A

Dominant suppressors (S-)

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14
Q

In what conditions are you able to see the effects of mutant phenotypes?

A

In a sensitized background (in sev hypomorphs) does the mutation have an effect on eye morphology

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15
Q

What genes play a part in establishing regional differences in the embryo that lead to the proper segment number?

A

maternal effect genes

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16
Q

Zygotic segmentation genes

A

expressed by the zygote’s own genome, subdivides the body into an array of essentially identical body segments

17
Q

Homeotic genes

A

a set of genes that encode transcription factors, assigns a unique identity to each body segment

18
Q

maternal effect mutations

A

recessive mutations in maternal genes that influence embryonic development

19
Q

Bicoidn (bcd)

A

The protein product that is a transcription factor whose mRNA is localized at the anterior tip of the egg cytoplasm that is translated after fertilization. It diffuses from the anterior end to produce a high-to-low, anterior-to-posterior concentration gradient that determines most aspects of the head and thorax development.

20
Q

morphagen

A

a substance that defines different cell fates in a concentration-dependent matter ex) bicoid is a morphagen

21
Q

What are the two ways in which bicoid works?

A

1) as a transcription factor that helps control the transcription of genes farther down the regulatory pathways
2) a translational repressor (targets transcript of the caudal (cad) gene)

22
Q

Caudal (cad) gene

A
  • higher conc. of the Cad protein at the posterior end of the embryo and lower concentrations toward the anterior
  • plays an important role in activating genes expressed later in the segmentation pathway to generate posterior structures
23
Q

Nanos (nos) genes

A

The nanos mRNA is localized to the posterior egg cytoplasm by proteins encoded by other maternal genes. It is translated during the early nuclear division stages. However, Nos protein functions only as a translational repressor. Targets maternally supplied transcript of the hunchback (hb) gene which is deposited in the egg during oogenesis and is distributed uniformly before fertilization.

24
Q

what are the three classes of zygotic segmentation genes?

A

1) gap genes
2) pair-rule
3) segment polarity gene

25
Q

The first zygotic genes to be transcribed

A

gap genes

26
Q

how do maternal transcription factor gradients ensure that the various gap genes are expressed in their broad zone at the proper position in the embryo?

A

Binding sites in the enhancers of the gap genes have different affinities for the maternal transcription factors

27
Q

Pair-rule genes

A

Encode transcription factors that are expressed in seven stripes in preblastoderm and blastoderm embryos. They generate more sharply defined sections.

28
Q

Functions to determine certain patterns that are repeated in each segment

A

Segment polarity genes

29
Q

What directly regulates certain segment polarity genes?

A

the transcription factors encoded by pair-rule genes initiate the pattern by directly regulating certain segment polarity genes and is maintained by interaction between various cell genes

30
Q

What are two of the segment polarity genes? What are they responsible for?

A

hedgehog (hh) and wingless (wg)

These proteins together with transcription factors are responsible for many aspects of segment patterning

31
Q

What are signal transduction pathways?

A

They enable a signal received from a receptor on the cell’s surface to be converted to a final intracellular regulatory response

32
Q

What regulates homeotic genes?

A

They are regulated by the hap, pair-rule and segment polarity genes

33
Q

homeotic mutations

A

cause particular segments or parts of them, to develop as if they were located elsewhere in the body

34
Q

mutations affecting segments in the abdomen and posterior thorax

A

bithorax complex (BX-C)

35
Q

mutations affecting segments in the head and anterior thorax

A

antennapedia complex (ANT-C)

36
Q

What are infra-abdominal (iab) mutations?

A

They are mutations affecting abdominal segments

37
Q

What is a homeobox?

A

region of sequence homology

38
Q

hox genes

A

clustered homeobox genes