Lecture 3 Flashcards

(54 cards)

1
Q

What were the earliest life forms on Earth?

A

Single-celled organisms.

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2
Q

What groups include early single-celled life?

A

Bacteria, Archaea, and single-celled eukaryotes.

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3
Q

Why are single-celled organisms important for understanding multicellularity?

A

They provide insight into how multicellularity evolved.

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4
Q

What is Valonia ventricosa?

A

A species of single-celled alga with a diameter of 1–4 cm.

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5
Q

What basic cellular components do single-celled organisms contain?

A

DNA/RNA for genetic information, a cell membrane, and cytoplasm for metabolic activity.

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6
Q

What types of metabolism can single-celled organisms exhibit?

A

Photosynthesis (e.g. cyanobacteria) and chemosynthesis (some archaea).

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7
Q

Can single-celled organisms exist at different sizes?

A

Yes, they can grow at all sizes.

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8
Q

What evolutionary step preceded true multicellularity?

A

The evolution of multicellular colonies.

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9
Q

Give an example of colonial organisms.

A

Cyanobacteria forming long chains of individual cells.

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10
Q

How many times has multicellularity evolved in eukaryotes?

A

Multiple times independently.

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11
Q

Which groups evolved multicellularity independently?

A

Animals, plants, multicellular fungi, and cellular slime moulds.

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12
Q

What does repeated evolution of multicellularity suggest?

A

There are strong evolutionary drivers favouring multicellularity.

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13
Q

From which ancestor did multicellular eukaryotes evolve?

A

The Last Eukaryotic Common Ancestor (LECA).

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14
Q

When did the last common ancestor of modern eukaryotes live?

A

During the Mesoproterozoic era, approximately 1.6–1 billion years ago.

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15
Q

How does the timing of LECA relate to multicellular algae?

A

It is roughly the same age as the oldest multicellular algae.

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16
Q

What is a key protective advantage of multicellularity?

A

Larger size reduces vulnerability to predation.

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17
Q

How does multicellularity buffer organisms from the environment?

A

Larger organisms are more stable against external environmental changes.

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18
Q

What biological capability does multicellularity enable?

A

The development of specialised cell types.

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19
Q

How many cell types do humans have?

A

Over 200 distinct cell types.

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20
Q

What question arises from cell specialisation?

A

What caused specialised cells to evolve?

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21
Q

What does the Flagellar Synthesis Constraint Hypothesis propose?

A

A trade-off between cell movement and cell division due to shared machinery.

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22
Q

what is the method for flagellar synthesis constraint hypothesis

A

The microtubule organising machinery needed for formation of
flagella is also required for the formation of spindle apparatus
used in cell division.

  • There is competition for the use of this machinery for the
    process of cell movement and cell division.
  • Presence of both specialised flagellated and non-flagellated cells
    in a simple colony allows the organism to move and grow at the
    same time
23
Q

Why are flagella important in simple multicellular organisms?

A

They allow the organism to move.

24
Q

What cellular machinery is shared between flagella and cell division?

A

Microtubule organising machinery.

25
Why does this shared machinery create a constraint?
It cannot be efficiently used for movement and division simultaneously.
26
How does cell specialisation solve this constraint?
Having both flagellated and non-flagellated cells allows movement and growth at the same time.
27
What is mosaic development?
A theory proposing unequal inheritance of genetic determinants during cell division.
28
Who proposed the idea of nuclear “determinants”?
August Weismann.
29
What experimental work challenged mosaic development?
Sea urchin experiments by Hans Driesch.
30
What did Driesch conclude about development?
All cells contain the full information needed for normal development.
31
Why is Dolly the sheep significant?
She demonstrated that differentiated adult cells retain full genetic information.
32
How was Dolly created?
By nuclear transfer from a mammal cell nucleus into an oocyte.
33
What concept did Dolly challenge?
The irreversibility of cell differentiation.
34
What does Dolly show that gene specialisation depends on?
It depends on gene expression, not gene content.
35
Who demonstrated the importance of cell signalling in development?
Hans Spemann and Hilde Mangold.
36
What was the key result of the Spemann–Mangold experiment?
Transplanted tissue caused the formation of a secondary embryo.
37
What can cell fate be influenced by?
interactions with neighbouring cells.
38
Why is balance of cell types important in multicellular organisms?
Too many of the wrong cell types prevents proper function.
39
Why must cell lineage depend on gene regulation?
All cells have the same genetic material.
40
What key process controls which genes are active during development?
Cell-to-cell signalling.
41
Why is signalling essential for homeostasis?
It allows regulation of the internal environment despite external changes.
42
What developmental processes require signalling?
Cell cycle regulation, movement, differentiation, and patterning.
43
Why must cells recognise self vs non-self?
To organise into a coherent multicellular structure.
44
Why is cell adhesion important?
It allows cells to form tissues, structures, and extracellular matrices.
45
What organisms are closely related to animals based on genome analysis?
Choanoflagellates.
46
Why are choanoflagellates important for understanding multicellularity?
They possess genes for signalling pathways found in animals.
47
What signallinh predates multicellularity?
Intercellular signalling predates multicellularity.
48
What are examples of cellular responses to signalling?
Cell movement, contraction, gene expression changes, metabolic changes, ion concentration changes, and protein activity changes.
49
What does gene expression cause that is especially important in development?
Changes in gene expression leading to cell specialisation.
50
What is gene expression
The process by which a gene’s coded information is converted into cellular structures or functions.
51
Does gene expression always produce proteins?
No, it can also produce functional RNAs such as tRNA, rRNA, and regulatory RNAs.
52
Why is the central dogma important for development?
It shows multiple points where gene expression can be regulated.
53
What experimental techniques are linked to this content?
End-point PCR, RT-qPCR, and Western blotting.
54
At what levels can gene expression be regulated?
Transcription, RNA processing (e.g. splicing), nuclear export, and post-translational modification.