Difference between Gene and Chromosome: Overview, Explanation

Difference between Gene and Chromosome: Overview, Explanation

Edited By Irshad Anwar | Updated on Nov 15, 2024 04:55 PM IST

The difference between genes and chromosomes lies in their roles in inheritance. A gene is a DNA segment that codes for specific traits, while a chromosome is a thread-like structure that carries many genes and organizes DNA. Understanding the comparison between the behaviour of chromosomes and genes is crucial. Genes control traits, while chromosomes ensure proper genetic material distribution during cell division. This is one of the important topics in genetics Biology class 12th.

This Story also Contains
  1. What is a Chromosome?
  2. Key Differences between Gene and Chromosome
  3. What is a Gene?
Difference between Gene and Chromosome: Overview, Explanation
Difference between Gene and Chromosome: Overview, Explanation

What is a Chromosome?

The chromosome is a thread-like structure composed of both DNA and proteins carrying the material. Chromosomes are located inside the nucleus of living cells, so in the real sense, it is crucial for the transmission of genetic material across generations. Each species has a characteristic number of chromosomes, and they are very instrumental in determining the traits and characteristics of an organism.

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Structure of Chromosomes

Chromosomes are made up mainly of DNA molecules that are tightly coiled around proteins called histones. In its coiled structure with protein, the DNA is called chromatin and condenses to visible structures during cell division. There are several characteristic regions on a chromosome:

  • A centromere is a specialised region where the chromatids are joined and to which the spindle fibres attach during cell division.

  • Telomeres are located in the end portions of the chromosomes and prevent them from deteriorating or joining neighbouring chromosomes.

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Types of Chromosomes

Chromosomes can broadly be divided into two types

  • Autosomal chromosomes: Non-sex chromosomes that carry all characteristics of the organism.

  • Sex chromosomes: This type of chromosome decides the sex of an organism. Normally human females have two X-chromosomes (XX), and males carry one X and one Y chromosome and in such fashion are known as XY chromosomal system.

Key Differences between Gene and Chromosome

It is important to distinguish the differences between genes and chromosomes in the areas of genetics and biology. Even though both are significant in the carrying of genetic information, they differ a lot in terms of size, content, and cell location, among others, in addition to having different roles concerning the aspects of inheritance and cellular activities.

Differences Between Gene and Chromosome

Aspect

Gene

Chromosome

Size

Relatively small

Larger, consisting of tightly coiled DNA and proteins

Composition

Segment of DNA

DNA and histone proteins

Number in a typical cell

Many (thousands to millions)

Fewer (typically pairs, e.g., 23 pairs in humans)

Location in cell

On chromosomes

Within the nucleus

Function

Codes for proteins or RNA molecules

Carries genetic information which involved in cell division and gene regulation

Role in inheritance

Directly influences traits and inheritance

Ensures proper distribution of genes during reproduction


What is a Gene?

Gene is the unit of heredity. It contains the information for making proteins and determining the characteristics of living things. Gene is a section of DNA separated in any one of the chromosome pairs, which specifies a particular protein or sometimes RNA molecule. Genes are not only the units for transferring traits from parent to offspring but also for governing many biological processes inside the cell.

Gene Structure

The typical gene components are discussed below:

Promoter: This is a region located upstream of the coding sequence of DNA. It is the place where the process of transcription is initiated. This means that it is the point where the beginning of the action of transferring the gene's DNA onto RNA is initiated.

Coding sequence: This is also called an exon and is that portion of the gene that comprises the working instructions in forming a protein or RNA molecule. The nucleotide sequence of A, T, C, and G in the coding region determines the amino acid sequence of the protein.

Regulatory sequence: They are found upstream or downstream from the coding sequences, controlling the activity of associated genes. The enhancers and silencers of a gene regulate when and to what degree its product is expressed.

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Frequently Asked Questions (FAQs)

1. What is the difference between a gene and a chromosome?

Genes are segments of DNA that contain the functional units necessary for making proteins or RNA molecules. Chromosomes are condensed structures composed of DNA and protein, which carry many genes.

2. How many genes are there in a chromosome?

The number of genes in a chromosome varies from species to species and also with the size of the chromosome. Generally, a chromosome can carry hundreds of thousands of genes.

3. Why chromosomes are considered to be significant in genetics?

Chromosomes are considered to be significant because they have the composition of genes which are the unit of heredity. They make genetic information be passed on correctly during cell division and cause the inheritance of traits.

4. How are the chromosomes and genes known to influence inheritance?

Genes are present on chromosomes that determine various traits inherited from parents. Variation in the gene as alleles and the mode of their distribution during reproduction sets the individual character and genetic diversity within a population.

5. What would be the consequence of chromosomal or gene abnormality?

Abnormality in chromosomes or genes will lead to some form of genetic disorder or disease. Such abnormalities may disturb normal cellular functions, thereby affecting development and health, and predisposing individuals to a variety of factors.

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