Structure of Chromosome
Note on Structure of Chromosome
In-depth Exploration of Chromosome Structure
Introduction to Chromosomes
A chromosome is a highly organized structure of DNA and proteins that is found within the nucleus of eukaryotic cells. The term "chromosome" is derived from the Greek words "chroma" (color) and "soma" (body), reflecting their ability to be stained by certain dyes. These structures are the carriers of the genetic material of an organism, which is passed down from one generation to the next.
Chromatin: The Building Material of Chromosomes
Chromatin is the complex of DNA and proteins, primarily histones, that makes up chromosomes. It exists in a dispersed, uncondensed state during the interphase of the cell cycle, allowing for DNA replication and transcription.
Types of Chromatin:
-
Euchromatin:
- A less condensed, loosely packed form of chromatin.
- Rich in gene concentration and is actively transcribed.
- Appears as lightly stained regions of the nucleus.
-
Heterochromatin:
- A more condensed, tightly packed form of chromatin.
- Contains fewer genes and is generally transcriptionally inactive.
- Appears as darkly stained regions of the nucleus.
DNA Structure: The Blueprint of Life
Deoxyribonucleic acid (DNA) is the molecule that contains the genetic instructions for the development, functioning, growth, and reproduction of all known organisms and many viruses.
- Double Helix: DNA has a double helix structure, resembling a twisted ladder. The two strands are antiparallel, meaning they run in opposite directions.
- Components: Each strand is a polynucleotide chain, consisting of:
- A deoxyribose sugar.
- A phosphate group.
- A nitrogenous base.
- Nitrogenous Bases: There are four types of nitrogenous bases:
- Adenine (A)
- Guanine (G)
- Cytosine (C)
- Thymine (T)
- Base Pairing: The two strands are held together by hydrogen bonds between the bases, following a specific rule: Adenine pairs with Thymine (A-T), and Cytosine pairs with Guanine (C-G).
Gene: The Functional Unit of Heredity
A gene is a specific sequence of nucleotides in the DNA that serves as the fundamental unit of heredity. Each gene carries the instructions for synthesizing a specific protein or functional RNA molecule, which in turn determines a particular trait or characteristic of the offspring.
Chromosome Compaction: Fitting DNA into the Nucleus
The DNA in a single human cell, if stretched out, would be about 2 meters long. To fit this enormous length of DNA into the microscopic nucleus, it must be tightly coiled and compacted. This process occurs in several hierarchical levels:
- Nucleosomes ("Beads on a String"): The DNA double helix is wrapped around a core of eight histone proteins, forming a structure called a nucleosome. This gives the chromatin a "beads on a string" appearance.
- Solenoid Fiber: The string of nucleosomes is further coiled into a more compact structure called a solenoid fiber or 30 nm fiber.
- Loop Domains: This 30 nm fiber is then organized into a series of loops that are attached to a central protein scaffold.
- Metaphase Chromosome: During cell division, the looped domains are further coiled and compacted to form the highly condensed metaphase chromosome, which is visible under a light microscope.
Structure of a Metaphase Chromosome
A replicated chromosome, as seen during metaphase, has a distinct and well-defined structure.
Chromatids:
- A metaphase chromosome consists of two identical, parallel strands called sister chromatids.
- Each chromatid contains one of the two identical DNA molecules produced during DNA replication.
- The sister chromatids are joined together at the centromere.
Centromere:
- The centromere is a constricted region of the chromosome that plays a crucial role in the segregation of chromosomes during cell division.
- It serves as the attachment point for the kinetochore, a protein complex to which the spindle fibers (microtubules) attach to pull the sister chromatids apart.
Telomeres:
- Telomeres are specialized structures found at the ends of linear chromosomes.
- They consist of repetitive nucleotide sequences and act as protective caps, preventing the ends of chromosomes from deteriorating or fusing with neighboring chromosomes.
Types of Chromosomes
Chromosomes can be classified based on the position of the centromere:
- Metacentric: The centromere is located in the middle, resulting in two arms of equal length.
- Submetacentric: The centromere is slightly off-center, leading to one shorter arm (p arm) and one longer arm (q arm).
- Acrocentric: The centromere is located near one end, resulting in a very short p arm and a much longer q arm.
- Telocentric: The centromere is located at the very end of the chromosome. Humans do not have telocentric chromosomes.
Functional Classification:
- Autosomes: These are the chromosomes that do not determine the sex of an individual. In humans, there are 22 pairs of autosomes.
- Sex Chromosomes (Allosomes): These chromosomes determine the sex of an individual. In humans, the sex chromosomes are X and Y. Females have two X chromosomes (XX), while males have one X and one Y chromosome (XY).
/Class-10/1_2_Structure_of_Chromosome.mdx