Human Anatomy & Physiology (11th Edition)
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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The eukaryotic chromosomes are linear DNA molecules with free 3'-OH and 5'-PO3- ends. DNA free ends are signals of double strand breaks, which are highly detrimental for the cell. Using the diagram below as a reference, describe structurally how telomeres resolve this problem. Make sure to highlight the interactions involved, the nature of the telomeric sequences and the correct nomenclature for the structure formed.

**Diagram Explanation:**
- The diagram illustrates the structure of telomeric DNA at the ends of eukaryotic chromosomes.
- **Telomeric DNA (green bar):** It consists of repetitive sequences. The sequence shown is TTGGGG TTGGGGT TGGGG, with the 5' to 3' direction labeled.
- **Non-telomeric DNA (gray bar):** It has the complementary sequence of AACCCTAACCCTAACCCCAACCCT, 3' to 5'.

**Formation of T-loop:**
- The telomere forms a protective loop structure called a T-loop.
- The 3' overhang (TTGGGG) invades the double-stranded region, pairing with the complementary strand.
- This invasion and looping back creates a displaced single strand, visually forming a loop.

**Structural and Functional Significance:**
- The T-loop structure protects chromosome ends from being recognized as DNA damage.
- The interactions between the telomeric sequences stabilize the loop, preventing unwanted degradation and fusion of chromosomes.
- This configuration is essential for maintaining genomic integrity.

Understanding this structural adaptation is crucial for insights into chromosome stability and cellular aging processes.
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Transcribed Image Text:The eukaryotic chromosomes are linear DNA molecules with free 3'-OH and 5'-PO3- ends. DNA free ends are signals of double strand breaks, which are highly detrimental for the cell. Using the diagram below as a reference, describe structurally how telomeres resolve this problem. Make sure to highlight the interactions involved, the nature of the telomeric sequences and the correct nomenclature for the structure formed. **Diagram Explanation:** - The diagram illustrates the structure of telomeric DNA at the ends of eukaryotic chromosomes. - **Telomeric DNA (green bar):** It consists of repetitive sequences. The sequence shown is TTGGGG TTGGGGT TGGGG, with the 5' to 3' direction labeled. - **Non-telomeric DNA (gray bar):** It has the complementary sequence of AACCCTAACCCTAACCCCAACCCT, 3' to 5'. **Formation of T-loop:** - The telomere forms a protective loop structure called a T-loop. - The 3' overhang (TTGGGG) invades the double-stranded region, pairing with the complementary strand. - This invasion and looping back creates a displaced single strand, visually forming a loop. **Structural and Functional Significance:** - The T-loop structure protects chromosome ends from being recognized as DNA damage. - The interactions between the telomeric sequences stabilize the loop, preventing unwanted degradation and fusion of chromosomes. - This configuration is essential for maintaining genomic integrity. Understanding this structural adaptation is crucial for insights into chromosome stability and cellular aging processes.
The model illustrates the formation of condensates during transcription, highlighting two main types: the Dynamic Promoter Condensate and the Transient Gene-Body Condensate.

**Dynamic Promoter Condensate:**
- **Enhancer:** A DNA sequence that facilitates the transcription of a particular gene.
- **Transcription Factor:** Proteins that bind to specific DNA sequences, controlling the rate of transcription.
- **Initiation Factors and Co-activators:** Assist in the assembly of the transcription machinery at the gene promoter.
- **Pol II (RNA Polymerase II):** An enzyme involved in transcribing DNA into messenger RNA.
- **Promoter:** A region of DNA where transcription of a gene is initiated.

The Dynamic Promoter Condensate is formed by the interaction of RNA Polymerase II, transcription factors, initiation factors, and co-activators at the promoter region, facilitated by the enhancer.

**Transient Gene-Body Condensate:**
- **Elongation and RNA Processing Factors:** These assist in the elongation phase during transcription and the processing of RNA.
- **P (Phosphorylation):** Represents the addition of a phosphate group, which is a crucial regulatory mechanism for transcription.

This figure shows an active transcription process where the transient gene-body condensate facilitates transcription elongation, aided by elongation and RNA processing factors and marked by phosphorylation.

Overall, this model explains how condensates form during transcription to facilitate gene expression and processing, with each type playing a distinct role in the transcription process.
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Transcribed Image Text:The model illustrates the formation of condensates during transcription, highlighting two main types: the Dynamic Promoter Condensate and the Transient Gene-Body Condensate. **Dynamic Promoter Condensate:** - **Enhancer:** A DNA sequence that facilitates the transcription of a particular gene. - **Transcription Factor:** Proteins that bind to specific DNA sequences, controlling the rate of transcription. - **Initiation Factors and Co-activators:** Assist in the assembly of the transcription machinery at the gene promoter. - **Pol II (RNA Polymerase II):** An enzyme involved in transcribing DNA into messenger RNA. - **Promoter:** A region of DNA where transcription of a gene is initiated. The Dynamic Promoter Condensate is formed by the interaction of RNA Polymerase II, transcription factors, initiation factors, and co-activators at the promoter region, facilitated by the enhancer. **Transient Gene-Body Condensate:** - **Elongation and RNA Processing Factors:** These assist in the elongation phase during transcription and the processing of RNA. - **P (Phosphorylation):** Represents the addition of a phosphate group, which is a crucial regulatory mechanism for transcription. This figure shows an active transcription process where the transient gene-body condensate facilitates transcription elongation, aided by elongation and RNA processing factors and marked by phosphorylation. Overall, this model explains how condensates form during transcription to facilitate gene expression and processing, with each type playing a distinct role in the transcription process.
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