Development iV Flashcards

1
Q

Define gene knockout

A

Where you remove a certain gene and observe for a homeotic transformation to take place.

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2
Q

Define potency

A

Defined as the range of ccell fates available to a cell or group of cells. Has similiar meaning to competency.

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3
Q

Define totipotency

A

The capacity for a cell or group of cells to give rise to all the cells of the embryo including the extraembryonic membranes and tissues.

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4
Q

Define pluripotency

A

Describes the ability of a cell to develop into the 3 primary getm cell layers of the embryo but CANNOT form extra-embryonic tissues such as the placenta.

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5
Q

Define bi-potency

A

This is the capacity of a cell or group of cells to gi rise to only two cell types.

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6
Q

Define Unipotent stem cells

A

capacity of a cell to give rise to just one cell type

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7
Q

Constriction of embryo’s using baby hair ligatures in amphibians and showed that up until the 16 cell stage, all 16 nuclei remained totipotent. Which scientist showed this?

A

Hans Spenmann

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8
Q

Which scientists were responsible for the first nuclear transplantation experiments in Xenopus?

A

Briggs and Kings

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9
Q

What did John Gurdon do

A
  • Expanded on the work of briggs and kings.

Succesfully cloned a frog using nuclei from somatic xenopus cells

Thus Gurdon was the first person to clone an amphibian.

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10
Q

Who were the first people to successfully clone the first mammal

A

Wilmut and Cambell.

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11
Q

State which parts of the embryo serve as a source of pluripotent embryonic stem cells.

A

Inner cell mass

Epiblast

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12
Q

Which cells make up the inner cell mass

A

The inner cell mass is made up of the epiblast and the primitive endoderm.

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13
Q

Where in the embryo can we harvest pluripotent embryonic stem cells

A
  • From the epiblast.

- these pluripotent cells can be maintained in culture indefinitley.

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14
Q

Give three uses of embryonic stem cells

A
  • Study in vitro development
  • Generate genetically modified animals
  • generate teratoma’s.
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15
Q

What are iPSC’s

A

These are a type of pluripotent stem cells that can be generated from adult somatic cells by genetic re-programming.

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16
Q

How were iPSCs produced

A

In 2006, introduction of 4 genes encoding transcription factors can convert mature differentiated adult cells iintro pluripotent stem cells.

17
Q

Give two applications of iPSCs

A
  • Induce pluripotent stem cells from patients suffering from diseases.
  • Induce pluripotent stem cells from patients for cell replacement therapies.