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Difference between Gene and Chromosome: Overview, Explanation

Difference between Gene and Chromosome: Overview, Explanation

Edited By Irshad Anwar | Updated on Jul 17, 2025 04:10 PM IST

Genes and chromosomes form the basis of the inheritance of genetic information. They play a major role in inheritance, DNA structure, and genetic information transfer. The Difference Between Gene and Chromosome, A Gene is a segment of DNA coding a specific trait. A Chromosome is a larger structure that organizes DNA and carries many genes. Genes and Chromosomes are central to the study of Principles of Inheritance and Variation.

This Story also Contains
  1. What is a Chromosome?
  2. Chromosomes Structure
  3. Types of Chromosomes
  4. What is a Gene?
  5. Gene Structure
  6. Key Differences between Gene and Chromosome
  7. MCQs on Genetics
Difference between Gene and Chromosome: Overview, Explanation
Difference between Gene and Chromosome: Overview, Explanation

Genes control traits, while chromosomes ensure proper genetic material distribution during cell division. Knowing how genes differ from chromosomes helps in studying laws of inheritance patterns, genetic disorders and molecular biology. They explain the principles of heredity through the transmission of traits from one generation to the next.

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. It is crucial for the transmission of genetic material across generations. Each species has a characteristic number of chromosomes. They are very essential in determining the traits and characteristics of an organism. In humans, there are 23 pairs of chromosomes, and their function is to carry genetic information, control body traits, and sex determination.

Chromosomes Structure

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 key characteristic regions on a chromosome:

  1. Centromere: A centromere is a specialized region where the chromatids are joined and to which the spindle fibers attach during cell division.

  2. Telomeres: These are located at the ends of the chromosomes and prevent them from damage or joining neighboring chromosomes.

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Types of Chromosomes

The chromosomes and their functions are divided into autosomes and allosomes. The autosomes control body traits, and the allosomes (sex chromosomes) determine the sex of an individual.

  • Autosomal chromosomes: Non-sex chromosomes that carry all characteristics of the organism. Humans have 22 pairs of autosomes.

  • Sex chromosomes: This type of chromosome decides the sex of an organism. In humans, females have two X chromosomes (XX). Males carry one X and one Y chromosome, forming the XY chromosomal system.

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. It specifies a particular protein or sometimes RNA molecule. A gene controls traits by undergoing gene regulation and gene expression, determining when and how proteins are made. 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 structure of a gene is organized into specific regions that control how a gene functions and expresses its product. These regions include promoters, coding sequences, and regulatory sequences. A gene-to-protein process happens by transcription and translation. The typical gene components are discussed below:

  1. Promoter: 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.
  2. 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.
  3. Regulatory sequence: They are found upstream or downstream from the coding sequences. It controls the activity of associated genes. The enhancers and silencers of a gene regulate when and to what degree its product is expressed.

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.

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

Visibility

Not visible under a microscope individually

Visible during cell division (mitosis/meiosis)

Example in Humans

Gene for eye color, height, etc.

Chromosome 21 (involved in Down Syndrome)

Types of Mutation Impact

Gene mutations affect specific traits or proteins

Chromosomal mutations can affect multiple genes

MCQs on Genetics

Question: Which of the following is the basic unit of heredity in living organisms?

  1. Genotype

  2. Phenotype

  3. Chromosome

  4. Gene

Answer: A gene is the basic unit of heredity. It is a segment of DNA that contains instructions for the production of a specific protein or functional RNA molecule. Genes are responsible for the traits and characteristics that are passed down from parents to offspring.

Hence, the correct answer is Option 4) Gene

Question: Which of the following is an example of a heritable trait?

  1. A scar on the skin

  2. Eye color

  3. A tattoo on the arm

  4. A sunburn

Answer: A) A scar on the skin is not a heritable trait since it is not determined by genes and cannot be passed down to offspring.

  • B) Eye colour is determined by genes and is therefore an example of a heritable trait.

  • C) A tattoo on the arm is not a heritable trait since it is not determined by genes and cannot be passed down to offspring.

  • D) A sunburn is not a heritable trait since it is not determined by genes and cannot be passed down to offspring.

Hence, Option 2 is the correct answer Eye colour

Question: Which of the following statements about DNA is correct?

  1. DNA is a double-stranded molecule made up of amino acids.

  2. DNA carries the genetic information in the form of genes.

  3. DNA is found only in the nucleus of cells.

  4. DNA is a protein that provides structural support to cells.

Answer: DNA (deoxyribonucleic acid) is a double-stranded molecule made up of nucleotides, not amino acids. It carries genetic information in the form of genes, which are specific sequences of DNA that provide instructions for the synthesis of proteins and other molecules. DNA is found in the nucleus of cells, but it can also be found in other cell organelles like mitochondria and chloroplasts. DNA is not a protein but a nucleic acid.

Hence, the correct answer is option 2) DNA carries the genetic information in the form of genes.

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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.

6. What is the relationship between genes and alleles?

Genes are the basic units of heredity, while alleles are different versions of the same gene. For example, the gene for eye color can have different alleles that result in blue, brown, or green eyes. Alleles of a gene occupy the same locus on homologous chromosomes.

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