Answer:
Xiao can use these structures to create a similarity matrix that enables to differentiate between synapomorphies and homoplasies
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Explanation:
A synapomorphy is a trait that has been inherited from the same ancestor, this trait enables to establish a relation of homology between two or more species; while a homoplasy is an analog structure that doesn't have homology.
Answer:
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/ dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.
1. The C. elegans embryo as a system to study cell division
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the syncytial gonad makes it possible to use RNA interference (RNAi) to generate oocytes whose cytoplasm is reproducibly (>95%) depleted of targeted essential gene products. Introduction of dsRNA rapidly catalyzes the destruction of the corresponding mRNA in many different systems. However, depletion of pre-existing protein is generally a slow process that depends on the half-life of the targeted protein. In contrast, in the C. elegans gonad, the protein present when the dsRNA is introduced is depleted by the continual packaging of maternal cytoplasm into oocytes (Figure 1). Since depletion relies on the rate of embryo production instead of protein half-life, the kinetics tend to be similar for different targets. By 36-48 hours after introduction of the dsRNA, newly formed oocytes are typically >95% depleted of the target protein.
Explanation:
The art of breathing in someway.
Answer:
<u>3) Uncontrolled cell division occurred as a result of gene mutations</u>
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Explanation:
Spontaneous modifications within the genome may occur during the process of cell division. When copies of the DNA inside the cell are made, these mutations cause errors; and can include small single nucleotide polymorphisms, and large scale additions or deletions across multiple genes.
Some, like somatic mutations, exist only inside vegetative (body) cells, that cannot be passed onto offspring. This is caused by several factors like
- UV radiation,
- chemical mutagens,
- infective agents
UV radiation damages strands of DNA, by causing dimers to form; here, consecutive nucleotide bases covalently bond instead of those on the complementary strand. This conformational change causes errors in DNA proofreading and repair mechanisms where bases are not well-incorporated into the strand- tumors (clumps of uncontrolled cell growth) may form, resulting in melanoma, a type of skin cancer.
