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Explain the advantage of the systems biology approach to studying cancer versus the approach of studying a single gene at a time.

Short Answer

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The system biology aims to understand the cause and treatment related to cancer caused by multiple factors. In contrast, the single gene's behaviour that influences cancer development is considered in the approach to study a single gene.

Step by step solution

01

System biology

The experimental science that uses computational methods to deal with the complex structure and properties of biological entities is called system biology.

Examples of biological systems whose interactions are studied in system biology are living organisms, organs, and cell (life's elementary unit). The analysis of gene expression patterns to treat cancer is the application of system biology to medicine.

02

Cancer

The group of disorders characterized by the tissue growth regulation caused by uncontrollable cell growth in the body parts is called cancer. Examples of treatment approaches for cancer are chemotherapy, radiation therapy, bone marrow transplant, cryoablation, and surgery.

Lifestyle (smoking and unhealthy diet), pathogen (bacteria and virus), genetic mutation, and other diseases like obesity and diabetes are common causes of cancer.

03

Advantage of system biology versus the single-gene study influencing cancer

The system biology focuses on multiple factors causing cancer, whereas these factors are ignored in the single-gene approach to study cancer rather than focus on a single gene.

The system biology approach does not study the isolated gene (cellular entity); instead, this approach considers the integrated system of multiple genes responsible for causing cancer.

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Most popular questions from this chapter

The model of globin gene evolution shown in Figure 21.14 suggests that an ancestral gene is duplicated and mutated to become ฮฑ- and ฮฒ-globin genes, and then each one was further duplicated and mutated. What features of the data set to support the model?

Below are the amino acid sequences (using the single-letter code; see Figure 5.14) of four short segments of the FOXP2 protein from six species: chimpanzee (C), orangutan (O), gorilla (G), rhesus macaque (R), mouse (M), and human (H). These segments contain all of the amino acid differences between the FOXP2 proteins of these species.

Use a highlighter to color any amino acid that varies among the species. (Color that amino acid in all sequences.)

  1. The C, G, R sequences are identical. Identify which lines correspond to those sequences.
  2. The H sequence differs from that of the C, G, R species at two amino acids. Underline the two differences in the H sequence.
  3. The O sequence differs from the C, G, R sequences at one amino acid (having V instead of A) and from the H sequence at three amino acids. Identify the O sequence.
  4. In the M sequence, circle the amino acid(s) that differ from the C, G, R sequences, and draw a square around those that differ from the H sequence.
  5. Primates and rodents diverged between 60 and 100 million years ago, and chimpanzees and humans about 6 million years ago. Compare the amino acid differences between the mouse and the C, G, R species with those between the human and the C, G, R species. What can you conclude?

Describe three examples of errors in cellular processes that lead to DNA duplications

WHAT IF? What evolutionary processes might account for prokaryotes having smaller genomes than eukaryotes?

Homeotic genes

(A) encode transcription factors that control the expression of genes responsible for specific anatomical structures.

(B) are found only in Drosophila and other arthropods.

(C) are the only genes that contain the homeobox domain.

(D) encode proteins that form anatomical structures in the fly.

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