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18 Feb 2019

Suggest a way to increase the number of neurons in Drosophila by manipulating developmental control genes such that a larger number of cells would differentiate into neurons. Which cells would be converted into neurons, i.e. which tissue would end up having fewer cells as a consequence of your manipulation?

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Keith LeannonLv2

18 Feb 2019

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Related questions

Which of the following statements is TRUE regarding sea anemones?

	None of the answer options is correct.
	Spongesânot sea anemonesâpossess what is considered to be the âsimplestâ nervous system found in animals.
	Because sea anemones are âsimpleâ organisms, these animals only possess motor neurons; sensory neurons or interneurons are never found in sea anemones.
	Although sea anemones possess ânet-likeâ nervous systems, these animals have brains located at their bases (near where they would attach to rocks).
	Although sea anemones lack definitive brains, they do possess ganglia that serve a similar function to the paired ganglia of flatworms.

Some people have low levels of calcium circulating in the blood, a condition known as hypocalcemia. While for many this disorder has little to no effect, for some it can be life-threatening. How could low levels of calcium harm an individual?

	Low levels of calcium would not have any effect on synaptic transmission.
	Low levels of calcium would cause sustained depolarization of the presynaptic cell.
	Low levels of calcium would result in fewer signals sent between the pre- and postsynaptic cell.

Cephalization is: the

	All of these choices are correct.
	development of a brain within the head of an animal.
	concentration of sensory organs within the head end of an animal.
	development of a âhead endâ in an organism.

Which of the following are TRUE about the resting membrane potential? (Select all that apply.)

	It results from voltage-gated sodium channels remaining open for long periods of time.
	It results from K⁺ ions diffusing out of the cell.
	It results from the sodium-potassium pump moving more Na⁺ ions out of the cell than K⁺ ions into the cell.

Afferent and efferent neurons differ in:

	their size.
	the directionality of the information they send.
	their pattern of myelination.

A neuron that responds to the environment is a(n):

	interneuron.
	homeostatic neuron.
	motor neuron.
	sensory neuron.

Which of the following is NOT the role of an interneuron?

	stimulating a muscle to contract
	conveying information from the internal environment of an animal
	relaying information from sensory to motor neurons
	maintaining homeostasis

Where are postsynaptic cell receptor proteins synthesized?

	the Golgi apparatus
	the lysosome
	the cytoplasm
	the rough endoplasmic reticulum

Inhibition of the flexor muscle during the knee-extension reflex is an example of:

	homeostasis.
	reciprocal inhibition.
	negative feedback.
	All of these choices are correct.

10.

What type of cells produce myelin for sensory neurons?

	pyramidal neurons
	glial cells
	melanocytes
	astrocytes

Summary

please!

Multipotent versus restricted

Morphologically detectable neural crest cells usually are first observed as the cells individualize and delaminate upon emigration from the neural tube, following their epithelial to mesenchymal transition (EMT), in which they convert from a tightly adherent sheet of cells to a dispersed and more individual mesenchymal population. Prior to EMT, however, it is difficult or impossible at most axial levels and in most species to distinguish presumptive neural crest cells from cells that will form dorsal neural tube derivatives. However, there are exceptions, such as a subpopulation of cranial neural crest cells in chick and mouse that appears to be set aside and morphologically distinct at midbrain levels. In addition, some species such as axolotl have a clearly segregated population of neural crest cells that exists as a ridge on the dorsal neural tube.

A long-standing debate in the neural crest literature has been whether neural crest cells are multipotent and/or restricted in their developmental potential. In other words, can a single neural crest precursor form only one type of derivative or are the cells multipotent and able to produce multiple derivatives. Single cell lineage experiments (Bronner-Fraser and Fraser, 1988), in which individual cells within the chick dorsal neural tube are labeled with vital dye, show that some of the labeled clones contribute to multiple differentiated cell types in the periphery, including melanocytes, sympathetic and sensory ganglion cells. Thus, the original precursor was âmultipotentâ in its developmental potential to form neural crest derivatives. In addition to neural crest derivatives, single dorsal neuroepithelial cell also give rise both to migrating neural crest cells and cells that remain in the dorsal neural tube, such as roof plate cells and dorsal sensory neurons and/or interneurons. This suggests a shared lineage between the neural tube and neural crest, at least at this stage. However, labeling migrating neural crest cells in vivo also produced clones that could contribute to more than one neural crest lineage (Fraser and Bronner-Fraser, 1991), again supporting the idea that some of the migrating population retained multipotency.

Clonogenic culture of neural crest cells cultured shortly after their emigration from the neural tube definitely shows that many early migrating neural crest cells are multipotent in vitro as well (Baroffio et al., 1988, Calloni et al., 2007, Calloni et al., 2009, LeDouarin et al., 2008a, LeDouarin et al., 2008b, Sieber-Blum and Cohen, 1980 and Stemple and Anderson, 1993). Exposure to different growth factors can profoundly influence their lineage decisions (e.g. Lahav et al., 1998). Furthermore, they have a capacity for self-renewal, at least for a few cell divisions (Stemple and Anderson, 1993 and Trentin et al., 2004).

The fact that individual neural crest cells can form multiple derivatives has led to the idea that they have stem cell properties. Stem cells are defined as individual progenitor cells that can generate one or more specialized cell types. A cardinal feature of stem cells is their ability to self-renew, that is, to divide so as to give rise to at least one daughter cell that maintains the multipotent character of its parent. The fact that cloned neural crest cells have a limited ability to self-renew has led to the idea that they are stem-like (progenitors) cells rather than true stem cells. Interestingly, however, neural crest stem cells can be derived from adult tissues (Fernandes et al., 2008 and Shakhova and Sommer, 2010; see Chapter Dupin and Sommer), suggesting that they can remain quiescent for long periods of time or maintain long term self-renewal ability when left in situ.

The presence of some multipotent neural crest precursors cannot, however, rule out the possibility that other precursors may be more restricted in their developmental potential. In fact, experiments in zebrafish suggested that neural crest cells contribute to different sets of derivatives accordingly to their migration order (Raible and Eisen, 1994). However, if the leader cell was ablated, the next cell in line took up the fate that would have been filled by the ablated cell (Raible and Eisen, 1996). Similarly, early migrating neural crest cells normally exhibit a broader range of derivatives than later migrating cells; however, when the early population is ablated and replaced by late migrating cells, the late migrating cells assume a broader developmental potential than that prescribed by their normal fate (Baker et al., 1997). This raises a very important issue: that developmental potential is greater than or equal to a cell's normal fate. Only by challenging the cell by putting it into a new environment can one test for restriction of cell fate. This is best exemplified by experiments in which the potential of neural crest populations was challenged by performing heterotopic transplants between different axial levels (LeDouarin and Teillet, 1974), such as exchanging cranial and trunk, or vagal and trunk populations. The results demonstrate a combination of flexibility in cell fate and some axial level-autonomous characteristics. For example, cranial neural crest cells normally make cartilage and bone of the face whereas trunk neural crest cells do not. Transplantation of cranial neural folds to the trunk results in production of many normal trunk derivatives, as well as the formation of ectopic cartilage nodules (Le Lievre et al., 1980 and LeDouarin and Teillet, 1974). Conversely, transplantation of trunk neural folds to the head results in contributions to cranial neurons and glia of cranial ganglia, but not to cartilage, although some connective tissues and pericytes derive from this graft (Nakamura and Ayer-le Lievre, 1982). This reveals some flexibility in fate, but a more limited ability to form skeletal derivatives (LeDouarin et al., 2004). However, trunk neural crest cells can form cartilage in vitro under appropriate culture conditions (Calloni et al., 2007 and McGonnell and Graham, 2002). Because challenging prospective neural crest fate is a difficult experiment, it is much easier to prove multipotency than restricted cell fate, leaving the question of whether or not there are lineage-restricted neural crest precursors still open to debate (see Krispin et al., 2010).

QUESTION 1

How is a bone marrow transplant able to treat someone with leukemia?

		The donor blood contains antibodies that destroy cancer cells
		Donor blood contains stem cells that regenerate cells in the immune system
		Bone marrow contains induced pluripotent stem cells that turn into red blood cells
		Bone marrow contains tumor supressor genes that slow down leukemia growth
		Bone marrow contains pluripotent human embryonic stem cells

1.2 points

QUESTION 2

What would happen if siRNAs designed to target mRNA from an oncogene were introduced into cancer cells?

		Increased genomic instability would result from adding foreign nucleic acids
		New mutations would arise in the oncogene
		The oncogene would be converted back into a proto-oncogene
		The siRNAs would compete with the oncogene's active site
		Production of the oncogene protein would decrease

1.2 points

QUESTION 3

What is the purpose of chromatin-remodeling enzymes in human cells?

		The enzymes control the rate of translation of an mRNA transcript
		The enzymes add phosphate or methyl groups to histone tails
		The enzymes slide nucleosomes farther apart or closer to each other
		The enzymes send damaged proteins to the proteasome for degradation
		The enzymes cause DNA looping to occur

1.2 points

QUESTION 4

If you wanted to resurrect the mammoth, how would you do it?

		Use somatic cell nuclear transfer to insert the mammoth genome into the egg of an elephant
		Use transcription factors to re-program adult cells from elephants into mammoth cells
		Change the gene expression patterns of elephants to increase production of mammoth genes
		Use siRNAs to decrease expression of elephant-specific genes in an elephant embryo

1.2 points

QUESTION 5

How is eukaryotic transcription initiated?

		RNA polymerase is recruited to the start codon by transcription factors
		RNA polymerase begins transcription at the enhancer sequence
		RNA polymerase is activated by binding to GTP
		An initiator tRNA binds to the ribosome
		A complex of proteins forms at the promoter of a gene