Neuro3 - 20 Flashcards

1
Q

What are the three developmental brain compartments?

A

Prosencephalon, mesencephalon, rhombencephalon

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2
Q

What does the prosencephalon become?

A

Telencephalon and diencephalon

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3
Q

What does the mesencephalon become?

A

Remains the same

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4
Q

What does the rhombencephalon become?

A

Metencephalon and myelencephalon

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5
Q

How is the neural tube patterned?

A

Activation-transformation

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6
Q

Outline activation-transformation

A

Neural-inducing molecules induce and maintain anterior forebrain, but only in the prechordal tissue; other signals, antagonised by the prechordal tissue, pattern posterior

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7
Q

Who and how was it determined that A-P neural patterning could be uncoupled?

A

Otto Mangold - late graft would only induce either A or P neural

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8
Q

What is anencephaly?

A

No forebrain

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9
Q

What acts to posteriorise the embryo?

A

Wnt, FGF and RA

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10
Q

What balances the posteriorising signals to maintain an anterior identity?

A

BMP and Wnt inhibitors

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11
Q

3 Wnt inhibitors

A

Cerberus, dickkopf, frzb1

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12
Q

How do posteriorising factors exert their action?

A

TFs called Hox genes

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13
Q

What does Hox stand for?

A

Homeobox

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14
Q

What does hox DNA code for?

A

Homeodomain of 60 a/a

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15
Q

What is the hox patterning system?

A

Conserved along AP axis in time and space

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16
Q

What is the hox-rhombomere effect?

A

Particular nerves derive from discrete rhombomeres in the hindbrain

17
Q

What is rhombomere formation caused by?

A

Hox expression

18
Q

What hox gene codes for the abducens nerve?

A

Hoxa1

19
Q

What transcription factors are expressed in the midbrain formation?

A

Otx2, and Gbx2 (posteriorly)

20
Q

What develops at the border of Otx2 and Gbx2 expression?

A

Isthmus - organiser type tissue