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15 Flashcards in this deck.
Chromosomes are thread-like structures located within the nucleus of animal and plant cells. Composed of DNA and proteins, they carry genetic information crucial for the growth, development, and reproduction of organisms. Each species has a characteristic number of chromosomes; for example, humans possess 46 chromosomes, arranged in 23 pairs.
Structure: Chromosomes consist of tightly coiled DNA wrapped around histone proteins, forming a complex known as chromatin. During cell division, chromatin condenses to form visible chromosomes, ensuring DNA is accurately distributed to daughter cells.
Function: Chromosomes ensure that DNA is replicated and distributed correctly during cell division. They play a critical role in heredity by transmitting genetic information from parents to offspring. Each chromosome contains numerous genes, which are specific sequences of DNA that code for proteins and determine various traits.
Types of Chromosomes: Humans have 22 pairs of autosomes and one pair of sex chromosomes (XX in females and XY in males). Autosomes carry genes responsible for most bodily functions, while sex chromosomes determine an individual's sex and can carry genes linked to sex-specific traits and disorders.
Genes are the basic units of heredity, segments of DNA that contain instructions for building proteins. These proteins perform a myriad of functions within organisms, influencing everything from physical appearance to cellular processes.
Structure: A gene consists of a specific sequence of nucleotides within a DNA molecule. Each gene has regions called exons, which code for proteins, and introns, which are non-coding regions that may regulate gene expression.
Function: Genes determine inherited traits by coding for proteins that contribute to an organism's structure and function. For example, the gene responsible for eye color produces proteins that affect pigment formation in the iris.
Gene Expression: The process by which a gene's information is used to synthesize a functional product, typically a protein. Gene expression involves transcription (copying DNA into mRNA) and translation (assembling proteins based on mRNA sequences).
Mutations: Changes in the nucleotide sequence of a gene can lead to mutations, which may alter protein function and potentially result in genetic disorders or variation within a population.
Nucleotides are the building blocks of nucleic acids, such as DNA and RNA. Each nucleotide comprises three components: a phosphate group, a five-carbon sugar, and a nitrogenous base.
Components:
DNA Structure: DNA is a double helix formed by two strands of nucleotides running in opposite directions. The sequence of nitrogenous bases encodes genetic information, with specific sequences corresponding to different genes.
Base Pairing: The specificity of base pairing (A with T and C with G) ensures accurate DNA replication and transcription. During replication, each strand serves as a template for creating a new complementary strand.
Genetic Code: The sequence of nucleotides in DNA is translated into the sequence of amino acids in proteins. Groupings of three nucleotides, called codons, correspond to specific amino acids or stop signals during protein synthesis.
DNA's structure is pivotal for its function in storing and transmitting genetic information. The double helix model, proposed by Watson and Crick, describes two complementary strands intertwined around a common axis.
Double Helix: The two strands of DNA are antiparallel, meaning they run in opposite directions. The sugar-phosphate backbone provides structural integrity, while hydrogen bonds between complementary bases hold the strands together.
Replication: DNA replication is a semi-conservative process where each original strand serves as a template for a new strand. Key enzymes involved include:
The replication process ensures genetic continuity across generations of cells, maintaining the integrity of the genetic information.
Genetic inheritance refers to the transmission of genetic information from parents to offspring. It follows specific patterns, primarily described by Mendelian genetics, which include dominant and recessive traits.
Mendelian Inheritance: Gregor Mendel's experiments with pea plants established the basic principles of heredity, including the concepts of dominant and recessive alleles and the segregation and independent assortment of genes.
Alleles: Different versions of a gene that determine distinct traits. An organism inherits two alleles for each gene, one from each parent.
Genotype and Phenotype:
Non-Mendelian Inheritance: Not all traits follow simple Mendelian patterns. Examples include incomplete dominance, codominance, polygenic inheritance, and mitochondrial inheritance, adding complexity to genetic predictions.
Advancements in genetic technologies have revolutionized the study and application of genetics. Techniques such as PCR, gene cloning, and CRISPR-Cas9 allow for precise manipulation and analysis of genetic material.
Polymerase Chain Reaction (PCR): A technique used to amplify specific DNA sequences, enabling detailed study and manipulation of genes.
Gene Cloning: The process of creating identical copies of a gene, which is essential for genetic engineering, research, and therapeutic applications.
CRISPR-Cas9: A powerful gene-editing tool that allows for precise modifications to DNA, offering potential treatments for genetic disorders and advancements in biotechnology.
These technologies have vast implications in medicine, agriculture, and research, highlighting the importance of understanding chromosomes, genes, and nucleotides.
Aspect | Chromosomes | Genes | Nucleotides |
---|---|---|---|
Definition | Thread-like structures of DNA and proteins carrying genetic information. | Segments of DNA that code for proteins. | Basic building blocks of nucleic acids, consisting of a phosphate, sugar, and nitrogenous base. |
Function | Ensure DNA replication and distribution during cell division. | Determine specific traits by coding for proteins. | Form the structural framework of DNA and RNA, storing genetic information. |
Components | DNA and histone proteins. | DNA sequences with exons and introns. | Phosphate group, five-carbon sugar, nitrogenous base. |
Number in Humans | 46 (23 pairs). | Approximately 20,000-25,000 genes. | Four types in DNA: A, T, C, G. |
Role in Inheritance | Carry multiple genes, ensuring their transmission to offspring. | Specific units of heredity responsible for individual traits. | Provide the sequences that make up genes. |
To better remember the base pairing in DNA, use the mnemonic "A Tall Couple Greet" where Adenine pairs with Thymine and Cytosine pairs with Guanine. For understanding chromosome numbers, associate humans with the number 46 by breaking it down into 23 pairs, including the sex chromosomes. Additionally, when studying gene expression, visualize the process as a two-step journey: transcription (DNA to mRNA) followed by translation (mRNA to protein).
Did you know that humans share approximately 60% of their DNA with bananas? This surprising fact highlights the fundamental genetic similarities among all living organisms. Additionally, the discovery of the CRISPR-Cas9 gene-editing technology has revolutionized genetic engineering, allowing scientists to modify genes with unprecedented precision. These advancements not only deepen our understanding of genetics but also pave the way for innovative medical treatments and agricultural improvements.
Students often confuse genes with chromosomes, thinking genes are the same as the thread-like structures that chromosomes are. Remember, genes are specific sequences of DNA located on chromosomes. Another common mistake is misunderstanding dominant and recessive alleles. For example, thinking that having two dominant alleles is the only way a dominant trait appears can lead to errors. Ensure you recognize that a single dominant allele is sufficient to express the dominant trait.