Problem 13
Question
A karyotype reveals the ____ of a single cell. a. base sequences b. chromosomes c. hereditary information d. clones
Step-by-Step Solution
Verified Answer
A karyotype reveals the chromosomes of a single cell.
1Step 1: Understanding Karyotype
A karyotype is a laboratory procedure that produces an image of an individual's chromosomes. The image typically displays the number and shape of chromosomes visible within the nucleus of a eukaryotic cell.
2Step 2: Identifying the Purpose of Karyotyping
The main aim of a karyotype is to detect chromosomal abnormalities or to determine sex by looking at the chromosomes present. Usually, it involves arranging chromosomes in a standardized format to observe characteristic number and band patterns.
3Step 3: Analyzing the Options
We need to evaluate each given option: a. base sequences (refers to nucleotide sequences), b. chromosomes (structures containing DNA), c. hereditary information (encompasses more than just chromosomal observation), d. clones (identical genetic copies).
Since karyotyping focuses specifically on the visualization and analysis of chromosomes, option b is the best fit.
4Step 4: Determining the Correct Answer
Based on the understanding that a karyotype shows the complete set of chromosomes of a single cell arranged in a particular order, the correct answer is: b. chromosomes.
Key Concepts
Chromosomal AbnormalitiesEukaryotic CellNucleus
Chromosomal Abnormalities
Chromosomal abnormalities are changes in the normal number or structure of chromosomes. These abnormalities can significantly affect the development and function of an organism. There are two main types of chromosomal abnormalities:
While some individuals with chromosomal abnormalities can live relatively healthy lives, others may experience severe developmental challenges or health issues. Regular karyotyping during prenatal screenings can provide crucial insights into the chromosomal health of a developing fetus.
- Numerical abnormalities: These occur when a cell has an unusual number of chromosomes. For example, Down syndrome is caused by an extra copy of chromosome 21, leading to a total of 47 chromosomes per cell instead of the usual 46.
- Structural abnormalities: These result from changes in the structure of a chromosome. Such changes may involve the deletion, duplication, inversion, or translocation of chromosome segments. For instance, a deletion might cause a loss of genetic material, while a translocation can lead to improper gene expression.
While some individuals with chromosomal abnormalities can live relatively healthy lives, others may experience severe developmental challenges or health issues. Regular karyotyping during prenatal screenings can provide crucial insights into the chromosomal health of a developing fetus.
Eukaryotic Cell
Eukaryotic cells are complex cellular structures characterized by their membrane-bound organelles, with the most prominent being the nucleus. Eukaryotic organisms include animals, plants, fungi, and protists.
Inside a eukaryotic cell, each organelle has a specific function, contributing to the cell's overall operation:
Inside a eukaryotic cell, each organelle has a specific function, contributing to the cell's overall operation:
- Nucleus: Contains the cell's genetic material and plays a central role in gene regulation and expression.
- Endoplasmic Reticulum: Involved in synthesizing proteins and lipids, and transporting them within the cell.
- Mitochondria: Known as the powerhouse of the cell, where cellular respiration occurs to create energy in the form of ATP.
- Golgi Apparatus: Modifies, sorts, and packages proteins for secretion or use within the cell.
Nucleus
The nucleus is often referred to as the control center of the eukaryotic cell. It houses the cell's chromosomes and is essential for regulating gene expression and maintaining genetic integrity.
Here's how the nucleus functions and its importance:
Here's how the nucleus functions and its importance:
- Chromosome Storage: The nucleus contains all of the cell's chromosomes, organized and compressed within a structure called chromatin. When preparing for cell division, chromatin condenses to form visible chromosomes.
- DNA Replication: Inside the nucleus is where DNA replication occurs, ensuring that each new cell receives a complete set of genetic instructions.
- RNA Synthesis: It is the site of transcription, where DNA is transcribed into messenger RNA (mRNA), which will be translated into proteins by ribosomes in the cytoplasm.
- Nuclear Envelope: The nucleus is surrounded by a double membrane called the nuclear envelope, which protects the genetic material and regulates the passage of molecules between the nucleus and the rest of the cell.
Other exercises in this chapter
Problem 11
The DNA of each species has unique ____ that set it apart from the DNA of all other species. a. nucleotides b. chromosomes c. sequencess d. bases
View solution Problem 12
_____ can be used to produce genetically identical organisms (clones) a. SCNT b. Embryo splitting c. Therapeutic cloning d. all of the above
View solution Problem 15
Match the terms appropriately. ______bacteriophage ______ clone ______nucleotide ______ diploid ______DNA ligase ______DNA polymerase ______ autosome a. nitroge
View solution Problem 10
______ is an example of reproductive cloning. a. Somatic cell nuclear transfer (SCNT) b. Multiple offspring from the same pregnancy c. Artificial embryo splitti
View solution