Early embryo development - cleavage stages Flashcards

(40 cards)

1
Q

Embryonic cleavage stages

A

= 1st divisions of embryo following fertilisation
-> mitotic cell cycles begin

Driven by maternal factors

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2
Q

Describe the divisions of the embryonic cleavage stages

A

No increase in overall volume

Short mitotic G1 & G2 phases
(cell growth)

Smaller daughter cells

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3
Q

Maternal factors

A

= factors inherited from oocyte
e.g. protein + mRNA

Asymmetrical inheritance
e.g. germ plasm

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4
Q

Blastomere

A

= embryo cell

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5
Q

Genesis of multicellularity

A

Follows fertilisation in developing embryo

  1. cleavage
  2. cell differentiation
  3. lineage allocation of embryonic cells
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6
Q

Cellular potency

A

= range of commitment options open to a given cell

e.g. pluripotent = give rise to all cell types

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7
Q

What happens to potency in blastomeres as time increases?

A

Potency decreases

-> different cells allocated different fates

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8
Q

Embryonic cleavage

- terminology

A

Cytokinesis
= cell division

Karyokinesis
= nucelar division

Cleavage furrow
= actomyosin ring that divides cells

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9
Q

2 types of embryonic cleavage

A

Holoblastic

Meroblastic

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10
Q

Holoblastic

A

Cleavage furrow completely separates
-> divides blastomeres
= complete cleavage

Sparse, uniform yolk distribution

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11
Q

Meroblastic

A

Only part of blastomere separated
= incomplete cleavage

Yolk impedes membrane formation

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12
Q

Sea urchin embryonic cleavage

A

Holoblastic divisions

- first 7 = stereotypic

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13
Q

Characteristics of sea urchin embryonic cleavage divisions

A

Divisions 1 + 2 = meridional
- pass through animal + vegetal poles

Division 3 = equatorial

Division 4 = cells of animal tier divide meridonally

Blastula = all cells same size

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14
Q

Sea urchin 60-cell embryo

A

Cell fates determined

2-step process in vegetal pole

Animal pole becomes ectoderm

Development through logic circuit of regulated TFs

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15
Q

2-step process in vegetal pole in sea urchin 60-cell embryo

A

Autonomous: maternal factors in large micrometer
-> becomes skeleton

Large micrometers then secrete paracrine factors
-> induce endoderm

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16
Q

Drosophila cleavage type

A

Meroblastic cleavage
= division plane doesn’t go completely through blastomere

Partial cleavage
= restricted to periphery

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17
Q

Drosophila cleavage stages

A

Karyokinesis occurs w/out cytokinesis
-> creates syncytium
(= many nuclei, 1 cytoplasm)

Cellular blastoderm = 6000 cells in <4hrs

18
Q

Drosophila cleavage

- mid-blastula transition

A

Embryonic gene transcription starts

  • initially inherits all maternal factors
  • > eventually needs to activate own genome
  • > switches on own TFs

Cycle 11: maternal mRNAs degraded

19
Q

Zebrafish cleavage type

A

Meroblastic cleavage
= cleavage doesn’t go all way through blastomere
- impeded by yolk

Cleavage restricted to thin region of animal pole
= blastodisc

20
Q

Zebrafish eggs

A

= teleoecithal

= mostly occupied by yolk

21
Q

Zebrafish

- mid-blastula transition

A

At cell cycle 10

= gene expression begins

22
Q

Xenopus cleavage type + symmetry type

A

Holoblastic cleavage
- egg has radial animal-vegetal symmetry

Mesolecithal
(=moderate yolk)
- displaced radial cleavage

23
Q

Xenopus eggs

A

Animal pole more heavily pigmented

region fertilised by sperm

24
Q

Fish embryo fate map

A

Polarised, non-uniform distribution of maternal factors
> pre-patterning
> arrangement of factors becomes 3 germ layers

25
Xenopus cleavage stages
Animal pole cleavage impeded by yolk | -> 2nd division starts in animal region before 1st division is finished
26
1st cleavage furrow imitation
Starts in animal pole Initiates with 20micrometre wide contractile band > actin filaments + myosin-II > assembled just beneath surface Surface initially forms periodic stress folds
27
1st cleavage furrow | - filopodia
Filopodia interact w/ opposing cell surfaces across cleavage furrow -> mediates blastomere-blastomere adhesion
28
1st cleavage furrow | -SA needed
Extra 20% SA needed
29
1st cleavage furrow | - motor
Actin-myosin motor
30
Localisation of maternal factors
Pre-patterning in oocytes If move factors from ectoderm to endoderm side -> different features develop in wrong places
31
Epigenetics | - DNA methylation
On 5-methylcytosine - lots of methylation in promoter region = switches gene off
32
Paternal and maternal genome demethylation
Tet3 catalyses oxidation - removes methyl groups Compartmentalisation means the 2 genomes are demethylated at different times
33
What does Tet3 do?
Oxidises 5mC to 5hmC/5fC/5caC
34
Early embryo transcript levels
Maternal mRNA levels decline after fertilisation -> mRNA degraded = stops being egg + starts being embryo
35
Embryonic gene activation What happens in species like zebrafish or frogs?
Embryo transcription initiates: > late 1-cell stage in mice > 4-cell stage in humans Mid-blastula transition -> more cells but similar time-frame
36
Lineage specification
= 1st embryonic differentiation Cell fate is dictated in a pre-determined way in asymmetric distribution of maternal factors
37
Lineage specification in mammals
Stochastic = changes randomly over time 2 lineages established: > trophectoderm - gives rise to extra-embryonic tissue: placenta + chorion > inner cell mass = gives rise to embryonic tissue
38
What are the lineage specifications in mammals driven by?
Driven by interplay between TFs Trophectoderm = Tead4 (Hippo signalling pathway) Cdx2 ICM = Nanog, Oct4, Essrb, Sox2
39
Molecules involved in lineage specification | - outside cells at 8-16 cell stage
Cdx2 levels increase - YAP dephosphorylated + enters nucleus with Tead4 - > Forms co-transcriptional complex - > Cdx switches off Oct4, Nanog + Sox2 = Trophectoderm
40
Molecules involved in lineage specification | - inside cells at 8-16 cell stage
Cdx2 levels decrease - > YAP is cytoplasmic - > Cdx2 increases Oct4, Nanog + Sox2 = Inner cell mass