Molecular Genetics and Early Embryonic Development- Bumann Flashcards

1
Q

cells begin to form specific and specialized structures

A

differentiation

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2
Q

cell divisions that form more cells with identical functions as the parent cells:

A

growth

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3
Q

What are the three stages of embryonic development?

A
  1. differentiation
  2. growth
  3. patterning
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4
Q

cells produced by cleavage get organized into layers and groups of cell masses through what is known as gastrulation:

A

pattterning

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5
Q

the process of patterning in which cells get organized into layers and groups of cell masses occurs through:

A

gastrulation

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6
Q

Patterning needs to occur in 3 dimensions, these include:

A
  1. anterior-posterior (top-bottom)
  2. dorsal-ventral (left-right)
  3. proximal-distal (front-back)
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7
Q

Where does fit in to the continuum of patterning and embryonic development?

A
  1. malocclusion syndromes
  2. craniofacial malformations
  3. bone mass traits
  4. tooth agenesis
  5. tooth movement
  6. tooth development disorders
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8
Q

The following conditions are all considered:

Pierre-Robin
Treater Collins
Marfan Syndrome

A

Malocclusion syndromes

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9
Q

The following conditions are all considered:

  • crouson
  • apert
  • pfierffer
  • cleating syndrome (lip & palate)
A

craniofacial malformations

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10
Q

The following conditions are all considered:

Sclerosterosis and van Buschem’s
High bone mass and OPPG
Paget’s syndrome

A

bone mass traits

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11
Q

Tooth Agenesis can be described as:

A

missing teeth

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12
Q

The following conditions are considered:

dentinogenesis imperfect
amelogenesis imperfecta

A

tooth development disorders

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13
Q

Amelogenesis imperfect can be described as:

A

tooth development disorder affecting the enamel

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14
Q

craniofacial anomalies account for:

A

1/3 of all congenital defects

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15
Q

Describe the susceptibility to teratogenesis during 0-2 weeks

A

not sensitive; high rate of lethality may occur

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16
Q

Describe the susceptibility to teratogenesis during 3-8 weeks

A

period of greatest sensitivity; each organ system also has a period of peak sensitivity

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17
Q

Describe the susceptibility to teratogenesis during 9-38 weeks

A

decreasing sensitivity; period of functional maturation

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18
Q

developmental time period in which the face is forming:

A

3-8 weeks

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19
Q

list four important concepts of embryonic development:

A
  1. universal mechanisms of animal development
  2. proteins can substituted across species
  3. inductive signaling
  4. regional determination
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20
Q

What are the five signaling pathways that species share in common?

A
  • receptor tyrosine kinase (RTK)
  • TGF-beta superfamily
  • WNT signaling
  • Hedgehog signaling
  • Notch signaling
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21
Q

multicellular organisms are enriched in proteins mediating:

A

cell interactions and gene regulation

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22
Q

Proteins can be ___ across species

A

substituted

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23
Q

_____ defines the development program of an organism

A

regulatory DNA

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24
Q

An important concept of embryonic development is ____vs. ___

A

asymmetric versus symmetric cell division

25
gradients reflective of a balance between positive and inhibitory inductive signals; sequential inductions
inductive signaling and morphogens
26
division in which sister cells are born different:
asymmetric division
27
division in which sister cells become different as result of influences acting on them after their birth
symmetric division
28
Inductive signaling is characterized by:
1. starting point (cell or cell cluster) 2. cell-cell signaling 3. cell signaling cascades 4. acts over great distances
29
Early developmental process in which the embryo (week 3 in humans) transforms from a single cell layer (blastula) into the three primary germ layers:
gastrulation
30
When does the process of gastrulation occur?
3 weeks in humans
31
gastrulation transforms a single cell layer (___) into three ___.
blastula; three primary germ layers
32
What are the three primary germ layers formed from the blastula through gastrulation?
- ectoderm - endoderm - mesoderm
33
Forms towards the anterior following gastrulation:
Hensen's Node
34
Forms from anterior to posterior following gastrulation:
primitive streak
35
Following gastrulation we get ____ formation towards the anterior and ___ formation towards the posterior:
head; somite
36
Race and ethnicity are considered ____ meaning they do not exist ___
social constructions; biologically
37
a socially defined category, based on real or perceived biological differences between groups of people:
race
38
a socially defined category based on common language, religion, nationality, history, or another cultural factor:
ethnicity
39
misappropriates the authority of science and undermines it by converting it into a social weapon:
scientific racism
40
the impact of social and environmental factors and how that manifests biologically to genetic changes in response to those stresses:
social epigenomics
41
Around how many distinct craniofacial syndromes are there?
more than 700
42
craniofacial syndromes are a significant cause of:
infant mortality
43
___ % of all live birth exhibit some form of minor or major craniofacial abnormality:
3%
44
embryonic cell population that is localized between the developing neural tube and the epidermis:
neural crest cells
45
Neural cells are an embryonic cell population located between:
the developing neural tube and the epidermis
46
Some neural crest cells exhibit ____ meaning that they can give rise to multiple differentiated cell types
"stemness"
47
In the formation of craniofacial structures (and many other structures) the ____ migrate through restricted pathways to form the developing structures
neural crest cells
48
Cell migration is a tightly regulated process and the NCCs receive cues such as ___ & ___ that restrict their movement and determine fate
morphogens & growth factors
49
over ___ genes have been identified that have mutations associated with tooth patterning morphogenesis defects and cell differentiation defects
300
50
As a collective group, ____ diseases are the most common
craniofacial genetic diseases
51
List the five categories of genetic diseases of the dentition:
1. ectodermal dysplasias 2. tooth agenesis 3. supernumerary teeth 4. cleft lip/ palate 5. skeletal diseases and the dentition
52
- greater than 100 different disorders - commonly involves one or more of teeth, nails, skin, sweat glands, and/or hair
ectodermal dysplasias
53
List the 3 types of tooth agenesis:
1. hypodontia 2. oligodontia 3. anodontia
54
Missing only a few teeth, common type of tooth agenesis
hypdontia
55
missing more than 6 teeth excluding third molars, more severe form of tooth agenesis
oligodontia
56
absence of teeth or complete lack of teeth
anodontia
57
form of tooth agenesis in which one or more teeth appear smaller:
microdontia
58
form tooth agenesis in which one or more teeth grow faster and exceed average size:
macrodontia
59
code that drives tooth formation & is extremely important that is results in the correct schematic
homeobox code