Briefly explain the role of chromosomes in heredity and its importance.
Solutions
Expert Solution
Chromosomes:
These are the vehicles which play a vital role in heredity by passing the traits from parents to offspring.
These are the thread-like structures which are composed of DNA and proteins.
These are found in the nucleus of cells.
Typically, humans have 46 chromosomes which are organized into 23 pairs with one set inherited from each parent.
Each of the chromosome contains numerous genes, that are segments of DNA which encode specific instructions for the development and functioning of an organism.
Genes are the units of heredity which are responsible for passing on traits or characters such as eye color, hair texture, and susceptibility to certain diseases.
During the process of sexual reproduction, the chromosomes undergo a crucial event called Meiosis.
Meiosis - this is a specialized form of cell division which occurs in reproductive cells i.e., sperm and eggs and results in the production of gametes i.e., sex cells with half the number of chromosomes that are found in other cells.
This reduction in chromosome number plays a vital role to ensure the proper number of chromosomes which is restored during fertilization.
During fertilization, when an egg and a sperm cell unite, each contributes half of the required chromosomes which results in a full complement of chromosomes in the offspring.
The combination of this genetic material from both the parents creates a unique genetic makeup for each individual.
The interaction and arrangement of genes on chromosomes determine how traits or characters are inherited.
The phenomenon of tendency of genes located on the same chromosome to inherit together is known as genetic linkage.
The genes can also undergo recombination during meiosis where the portions of the genetic material are exchanged between the chromosomes.
This recombination contributes to the genetic diversity and the generation of new combinations of traits or characters in the offspring.
The changes in the DNA sequence known as mutations also occur in chromosomes.
These alterations or changes may be inherited and can lead to variations in the traits or the development of genetic disorders.
Chromosomes:
These are the carriers of genes and they serve as the vehicles for passing genetic information from parents to offspring.
These are known as the Physical basis of heredity.
The two types of chromosomes are:
Autosomes & allosomes
Sex chromosomes & allosomes
Sex chromosomes & autosomes
X & Y chromosomes
In an autosomal inheritance where dominant gene is expressed,
all offspring will show dominant homozygous if:
Trait is sex-linked
Both parents are dominant homozygous
Both parents are dominant heterozygous
One of the parent is dominant heterozygous
In a sex-linked hemophilia disease due to a recessive gene, a
mating of homozygous female non-hemophilia with hemophilia male
will result in:
100%...
Where in the eukaryotic cell are the chromosomes found?
_________________________________________________
How many chromosomes are there in a human body (somatic) cell?
____________________
How many chromosomes are there in a human gamete?
__________________
If in some species the number of chromosomes in a diploid body
cell is 12 then the number of chromosomes in a haploid cell is
____________________.
The process of mitosis produces how many offspring (or
daughter) cells? ____________ These cells are clones of each
other.TRUEFALSE
The process of...
Why the process of licensing is necessary for replication of
eukaryotic chromosomes but not prokaryotic chromosomes? Describe
the main steps of licensing process.
1. Which statement is true of the behavior of chromosomes in
mitosis?
All chromosomes are duplicated during interphase, except for the
sex chromosomes
If the original number of chromosomes was 46 each daughter cell
will receive 23
Each new cell receives copies of all the original chromosomes
The daughter cells will be unique due to crossing over
2. Which of the following groups of molecules all function
primarily as a source of energy for a typical eukaryotic
cell?
Glycogen, Nucleic...
If a diploid cell is 2N=8, draw the chromosomes of the
following. How many chromosomes and chromatids would you see on the
cells in the following stages.
a) Nullisomic for chromosome 2 in G1
b) Monosomic for chromosome 1 in G1
c) Tetrasomic for chromosome 4 in mitotic metaphase
d) Trisomic for chromosome 2 in G2
e) Triploid in metaphase 1 of meiosis