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Chromosomes are the molecular architects of life, intricate structures within our
cells that carry the genetic information necessary for the development for
functioning of all living organisms. This document aims to delve into the
fundamental aspects of chromosomes, from their structure to their pivotal
functions in heredity and beyond.

Chromosomes are thread-like structured found within the nucelus in every cell
composed of dna and proteins, they act as carriers of genes - the units of
heredity. The DNA in chromosomes contains instructions necessary for growth,
development and functioning

The structure of chromosomes is a marvel of nature, dna, organised as a double


helix is tightly wound around histone proteins, forming nucleosomes. These
nucleosomes further coil and fold creating the structure.

Chromosomes are classified into two types - autosomes and sex chromosomes
Autosomes determine general traits, while sex chromosomes determine an
individuals biological sex.

Humans possess 23 pairs of chromosomes, totalling 46. One from each parent,
carry similar genetic information. The unique combination of genes determines
individual characteristics

Chromosome replication is a crucial process before cell division. Mitosis ensures


the faithful duplication and distribution of chromosomes in somatic cells, while
meiosis, occurring in germ cells is essential for sexual reproduction and genetic
diversity

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Genes located on chromosomes are the instructions for synthesising proteins and
controlling cellular functions, alleles, different versions of a gene and contribute to
genetic variation within populations

Chromosomal abnormalities can lead to genetic disorders, conditions like Down


syndrome caused by an extra copy of chromosome 21, underscore the delicate
balance required for proper development

Chromosomal mutations play a pivotal role in the process of evolution. Changes in


chromosome structure or number contribute to genetic diversity, enabling
adaptability in new environments.

Modern techniques like fluorescence in situ hybridisation and comparative


genomic hybridisation allow scientists to visualise and analyse chromosomes at a
molecular level. genome sequencing provides a comprehensive understanding of
an individuals entire dna.

Emerging technologies including crispy gene editing, hold promise for


manipulating chromosomes for therapeutic purposes. The integration of
chromosomal information into personalised medicine is poised to revolutionise
healthcare.

Chromosomes are the cornerstone of genetics and the key to understanding the
intricacies of life, their structure, function and the information.

1.What is the primary function of chromosomes in a cell.

Chromosomes are the carriers of genes. The DNA within chromosomes contains
instructions that are necessary for growth, development and functioning.

2. How many chromosomes are typically found in human somatic cells?

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46 total chromosomes

3. Name the cell division process that involves the separation of chromosomes
into daughter cells

Mitosis

4. True or False: Chromosomes are composed of DNA and proteins

True

5. Define function of the homologous chromosomes

They allow for the recombination and random segregation of genetic material from
the mother and father into new cells

6. During which phase of the cell cycle do chromosomes replicate?

S phase

DIPLOID CELL

H
R

CODOMINANT
M

O
S PHASE

O
M

1. cell that contains two sets of chromosomes

2.

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3. Genetic inheritance pattern where both alleles are expressed equally.

4.

5.

6. Phase where growth and reproduction happe

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