Autosomes and allosomes are important genetic terms which define the variation that exists in the number of chromosomes carrying genetic traits and constitute an individual's genetic makeup. These terms are discussed in the chapter Principles of Inheritance and Variation, class 12. This article includes the difference between autosomes and allosomes, their functions, and their role in inheritance. Understanding autosomes and allosomes helps form the core base of genetics which is important for competitive exams like NEET where Biology is one of the major subjects asked.
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Autosomes are chromosomes that do not determine sex. In the human body, they exist in 22 pairs, carrying most of the genetic information on traits such as eye colour, blood type, and metabolism. They are the same in males and females and are determined by size and structure. General body functions and development mainly depend on autosomes. Changes in autosomes may cause several genetic disorders.
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Allosomes or sex chromosomes are the chromosomes responsible for the determination of sex in an organism. Human beings have one pair of allosomes bearing two X chromosomes in females and one X and one Y chromosome in males. Such chromosomes carry genes not only for sexual characters but also for other sex-linked traits like colour blindness and haemophilia.
Autosomes and Allosomes are one of important topics among the differences and comparison articles in Biology. The table below describes the major difference between autosomes and allosomes:
Autosomes | Allosomes | |
---|---|---|
Number | 22 pairs in humans. | 1 pair in humans. |
Role in Sex Determination | Not involved in sex determination. | Determines sex (XX in females, XY in males). |
Presence | Same in both sexes. | Differs between sexes. |
Genetic Role | Carries genes for general traits and metabolism. | Carries genes for sex-linked traits. |
Inheritance Pattern | One from each parent, equally inherited. | Males inherit X or Y from their father, and X from their mother. |
Variation Among Species | The number remains similar in most species. | Varies widely among species. |
Mutation Effects | Mutations can lead to metabolic or structural disorders. | Mutations often lead to sex-linked disorders (e.g., colour blindness). |
Chromosome Size | Generally larger and more stable. | Y chromosome is smaller and more prone to mutations. |
Autosomes and allosomes complement each other in genetics. While autosomes are involved in determining the general phenotype as they carry genes responsible for most traits, allosomes are significant in determining sex and hence associate characters. In this sense, it is also crucial in explaining why some genetic disorders like Turner syndrome or Klinefelter affect the allosomes and hence influence sex characteristics.
The concept of autosome and allosome is important for students studying biology at class 12 and NEET levels in understanding the concepts of inheritance, genetic variation, and disorders. Thus, autosomal and allosomal knowledge form the basis of advanced topics that include chromosomal abnormalities, sex-linked inheritance, and genetic counselling.
Autosomes and allosomes are components of chromosomes.
They can be located in the genome of an organism.
In both, DNA and proteins are present.
They include details about a person's forebears.
They both possess genes.
They are found in pairs.
Anomalies in both types of chromosomes can lead to many genetic diseases.
Autosomes are chromosomes that are devoid of any sex-specific genes.
Due to the homomorphism of autosomes, the centromere is located in the same place.
On autosomes, there are 200–2000 different genes. In humans, chromosome 1 is the biggest chromosome and contains over 2800 genes.
The majority of chromosomes in a genotype are autosomes.
On the chromosomes of both men and women exist sex-determining genes (but may also carry many other genes that have nothing to do with sex).
Due to heteromorphic sex chromosomes, the position of the centromere varies between male and female chromosomes. Both male and female chromosomes have the same location for the centromere.
Here are some effective tips to prepare for the topic of Autosomes and Allosomes:
Study Aids: Examine the diagrams and features of autosomes and allosomes, including how autosomes comprise total traits in a species and how allosomes determine sex. Notice the examples: the ways in which human sex chromosomes are different, such as XX vs. XY.
Mnemonics: Try using mnemonics to help remember to differentiate between autosomes and allosomes: "GAS" for General traits (Autosomes) and Sex traits (Allosomes).
Practice Diagrams: Draw and label diagrams for autosomes and allosomes and display how they appear in males and females. Do this to achieve your understanding of structural differences.
Key Features: Note the particular functions of autosomes in body functions and the roles that allosomes play in sex-linked traits. When you know them you'll be better at answering the fine details.
The table below indicates the weightage and types of questions asked from autosomes and allosomes in different exams:
Exam Type | Types of Questions | Weightage |
---|---|---|
CBSE Exams | Short answer questions on the differences between autosomes and allosomes, with examples | 3-5% |
NEET | Multiple-choice questions (MCQs) on the structure and roles of autosomes and allosomes | 2-3% |
AIIMS | Assertion and reasoning questions on inheritance patterns and functions of autosomes and allosomes | 2-3% |
Nursing Exams | True/False questions on the number, role, and impact of autosomes and allosomes | 1-3% |
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Autosomal chromosomes function by carrying genes that encode for a wide range of traits and metabolic processes essential for an organism's development and maintenance. They are involved in various cellular functions, including growth, immune response, and metabolic activities. Autosomal chromosomes operate through the expression of these genes, influencing physical traits and physiological functions without determining the sex of the individual.
Yes, women possess 46 chromosomes in total, which include 22 pairs of autosomes and one pair of sex chromosomes (XX). Therefore, women have 44 autosomes (22 pairs) and 2 sex chromosomes, making up the complete set of 46 chromosomes.
Yes, the XXY chromosome configuration does exist. This chromosomal pattern is known as Klinefelter syndrome, a genetic condition that affects males. Individuals with Klinefelter syndrome typically have one extra X chromosome, resulting in a total of 47 chromosomes (44 autosomes and 3 sex chromosomes: XXY). This condition can lead to various physical and developmental traits, including reduced testosterone levels, gynecomastia and fertility issues.
Allosomes are sex chromosomes that are different in shape, size, or behaviour from a typical autosome. A typical pair of allosomes is the human sex chromosomes. In contrast to sperm, which can include either X or Y chromosomes, the X chromosome is present in the ovum.
Haploid and diploid cells both include autosomes. Chromosomes called autosomes don't affect sex determination. Human body cells are diploid, which means they contain two sets of autosomes—one from the mother and one from the father.
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