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What do SINE and LINE mean in terms of chromosome struc- ture? Why are they called "repetitive"?

Short Answer

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Answer: SINEs (short interspersed nuclear elements) and LINEs (long interspersed nuclear elements) are types of transposable elements (TEs) found in chromosome structure. They contribute to genome size, diversity, and evolution. They are called "repetitive" because they can duplicate themselves and insert the copies at multiple locations within the genome, leading to the accumulation of a large number of SINE and LINE sequences in genomic DNA.

Step by step solution

01

Definition of SINE and LINE

SINEs (short interspersed nuclear elements) and LINEs (long interspersed nuclear elements) belong to a class of DNA sequences known as transposable elements (TEs). TEs can move and duplicate themselves within the genome, which can result in the creation of new, repetitive DNA sequences. SINEs are relatively short sequences, usually less than 500 base pairs long, while LINEs are longer, ranging from 6,000 to 8,000 base pairs long.
02

SINE and LINE in Chromosome Structure

SINEs and LINEs are found scattered throughout the chromosomes. They do not code for proteins; instead, they play various roles in chromosome structure and function. For example, they contribute to genome size and diversity, the formation of new genes, and the regulation of gene expression. They can also act as a buffer during recombination events and enable the genome to adapt to changing environmental pressures. Furthermore, SINEs and LINEs can influence the overall three-dimensional organization of chromosomes within the cell nucleus.
03

Repetitive Nature of SINE and LINE

SINEs and LINEs are called "repetitive" because they can occur multiple times, often in tandem, within a particular chromosome. These repetitive sequences arise through the process of transposition, where SINEs and LINEs duplicate themselves and insert the copied sequences elsewhere in the genome. Over time, these events lead to the accumulation of a large number of SINE and LINE sequences within the genome. In humans, repetitive elements like SINEs and LINEs make up almost half of the genomic DNA. In conclusion, SINEs and LINEs are types of repetitive DNA sequences found in chromosome structure, which contribute to genome size, diversity, and evolution. They are called "repetitive" due to their ability to duplicate themselves and insert the copies at multiple locations within the genome.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

SINEs and LINEs
SINEs and LINEs are fascinating components of our genome. Standing for short interspersed nuclear elements (SINEs) and long interspersed nuclear elements (LINEs), these are specific types of transposable elements. Transposable elements are sequences of DNA that can move within the genome. This movement leads to potential changes in the genetic code and plays a significant role in shaping genetic information.
Both SINEs and LINEs are key contributors to the makeup of our DNA, with LINEs being much longer, ranging from 6,000 to 8,000 base pairs long, compared to the shorter SINEs, which are typically less than 500 base pairs. Despite their differences in length, both can impact genetic structure and function.
  • SINEs: Short, abundant, and non-coding
  • LINEs: Longer, can encode proteins to facilitate their own movement

The repetitive nature of these elements, through the process of transposition, enables them to occupy large portions of the genome. They have an interesting role in evolution and diversity due to their ability to multiply and insert themselves into new genomic locations.
Chromosome Structure
Chromosomes are the organized structures of DNA and proteins found within cells. They carry genetic information crucial for inheritance and biological functions. SINEs and LINEs, filling a significant portion of our chromosomes, contribute to their complex structure.
These elements do not just exist passively; they play active roles in maintaining and modifying chromosome integrity. Through evolutionary processes, the presence of SINEs and LINEs within chromosomes has offered genetic material a flexible means to adapt and evolve.
When these elements move, they can encourage genetic recombination or even influence how tightly chromosomes are packaged within the nucleus. Such structural modifications can have wide-reaching effects, not only on genetic health but also on the regulation of other genes.
  • Act as buffers or spacers during genetic recombination
  • Contribute to chromosomal architecture within the nucleus
Repetitive DNA Sequences
In the context of genomes, repetitive DNA sequences are patterns of nucleic acids that appear multiple times within the DNA molecule. SINEs and LINEs are among the most prolific contributors to this repetitiveness in human genomes.
This repetition is a result of their transposable nature, with copies being made and inserted throughout the DNA. The prevalence of these repeated sequences cannot be understated—nearly half of our DNA is composed of such repetitive elements.
Repetitive sequences like these are evolutionarily significant. They allow for genetic flexibility and adaptability, providing a reservoir of sequences that can be co-opted for new functions. While these sequences do not directly code for proteins, their presence can regulate important biological processes.
  • Significant portion of genomic DNA
  • Source of genetic variability and adaptation
Genome Diversity
The genome is the complete set of DNA within an organism, and its diversity is what allows for variation between individuals and species. SINEs and LINEs have a profound effect on this diversity due to their ability to move and replicate.
Their transpositions can change the arrangement and presence of genetic material, leading to new genetic combinations each generation. The resulting genetic shuffling can uncover advantageous traits, contributing to adaptation and evolution.
  • Increases genetic variation
  • Facilitates evolution by creating novel genetic arrangements

In this way, the activity of SINEs and LINEs look beyond mere repetition, becoming a driving force in the diversity that is foundational to life.
Gene Expression Regulation
Gene expression regulation is a crucial biological process that dictates how a cell uses its genetic code to produce proteins and perform its functions. SINEs and LINEs, while non-coding, are surprisingly influential.
Their presence within the genome can impact when and where genes are expressed. Through insertion near or within genes, they can alter gene regulation patterns, shifting how proteins and other molecules are made.
This regulation is essential, as it determines how cells react to and process biological signals. For instance, LINEs may carry promoter elements which can control the transcription of nearby genes. On the other hand, SINEs might disrupt a gene’s coding sequence or regulatory regions, leading to altered expression.
  • Modulate gene expression by acting on regulatory regions
  • Impact cell functioning by influencing transcription levels

Thus, these humble, repetitive elements hold sway over the intricate dance of molecular biology, guiding when and how genes manifest their effects in the body.

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Most popular questions from this chapter

What genetic process is occurring in a puff of a polytene chromosome?

While much remains to be learned about the role of nucleosomes and chromatin structure and function, recent research indicates that in vivo chemical modification of histones is associated with changes in gene activity. For example, Bernstein and others (2000. Proc. Natl. Acad. Sci. USA 97: 5340-5345) determined that acetylation of \(\mathrm{H} 3\) and \(\mathrm{H} 4\) is associated with 21.1 percent and 13.8 percent increase in yeast gene activity, respectively, and that yeast heterochromatin is hypomethylated relative to the genome average. Speculate on the significance of these findings in terms of nucleosome- -DNA interactions and gene activity.

In an article entitled "Nucleosome Positioning at the Replication Fork," Lucchini and others (2002. EMBOJ. 20: 7294-7302) state, "both the 'old' randomly segregated nucleosomes as well as the 'new' assembled histone octamers rapidly position themselves (within seconds) on the newly replicated DNA strands." Given this statement, how would one compare the distribution of nucleosomes and DNA in newly replicated chromatin? How could one experimentally test the distribution of nucleosomes on newly replicated chromosomes?

Define satellite DNA. Describe where it is found in the genome of eukaryotes and its role as part of chromosomes.

Mammals contain a diploid genome consisting of at least \(10^{9}\) bp. If this amount of DNA is present as chromatin fibers, where each group of 200 bp of DNA is combined with 9 histones into a nucleosome and each group of 6 nucleosomes is combined into a solenoid, achieving a final packing ratio of \(50,\) determine (a) the total number of nucleosomes in all fibers, (b) the total number of histone molecules combined with DNA in the diploid genome, and (c) the combined length of all fibers.

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