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Describe the structure of giant polytene chromosomes and how they arise.

Short Answer

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Short Answer: Polytene chromosomes are large, easily visible chromosomes that result from multiple rounds of DNA replication without cell division, a process called endoreplication. They consist of many parallel copies of chromatids, forming a unique structure with alternating bands and interbands, which represent tightly packed and less condensed chromatin regions, respectively. Polytene chromosomes play important roles in gene organization and regulation in certain specialized cells, such as those found in fruit flies and some mammalian cells.

Step by step solution

01

Introduction to Regular Chromosomes

In eukaryotic cells, genetic information is tightly packaged into structures called chromosomes, composed of DNA and associated proteins. Chromosomes are the structures in which genes are organized, and their proper structure and function are critical for the accurate transfer of genetic material during cell division.
02

Polytene Chromosomes

Polytene chromosomes are giant chromosomes found in certain cells of some organisms, such as fruit flies (Drosophila melanogaster). Unlike regular chromosomes, polytene chromosomes consist of multiple copies of homologous chromatids lying in parallel along the same axis. This unique structure makes them much larger and more easily visible under a light microscope compared to regular chromosomes.
03

Structure of Polytene Chromosomes

The unique structure of polytene chromosomes is primarily due to the presence of many repeated, parallel copies of chromatin strands that are aligned and closely packed together. The chromatin strands consist of DNA and histone proteins. These DNA copies remain closely associated, forming a structure called a chromonema. The repeated chromatids in a polytene chromosome are a result of repeated DNA replication cycles without cell division (also known as endoreplication). Furthermore, polytene chromosomes are characterized by alternating light and dark bands called interbands and bands, respectively. The bands represent regions of the chromosome with tightly packed chromatin, whereas the interbands represent regions with less condensed chromatin, where active genes are typically located.
04

How Polytene Chromosomes Arise - Endoreplication

Polytene chromosomes arise through a process called endoreplication or endoreduplication. In this process, the cells undergo multiple rounds of DNA replication without the mitotic cell division that normally follows replication. As a result, the cell's genome becomes amplified, causing the formation of these large, multiple copies of chromatids. This process can serve various purposes; for example, in the case of fruit flies, it allows certain tissues to grow and differentiate rapidly. While less common in vertebrates, some mammalian cells, such as trophoblast giant cells in the placenta and megakaryocytes in bone marrow, also contain polytene chromosomes due to endoreplication. In conclusion, polytene chromosomes are giant chromosomes formed through endoreplication, containing many parallel copies of chromatids. Their unique structure, consisting of alternating bands and interbands, plays a significant role in the organization and regulation of genes within certain specialized cells.

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Most popular questions from this chapter

The human genome contains approximately \(10^{6}\) copies of an Alu sequence, one of the best-studied classes of short interspersed elements (SINEs), per haploid genome. Individual Alu units share a 282 -nucleotide consensus sequence followed by a \(3^{\prime}\)-adenine-rich tail region (Schmid, 1998 ). Given that there are approximately \(3 \times 10^{9}\) base pairs per human haploid genome, about how many base pairs are spaced between each Alu sequence?

Describe the basic structure of a nucleosome. What is the role of histone H1?

Examples of histone modifications are acetylation (by histone acetyltransferase, or HAT), which is often linked to gene activation, and deacetylation (by histone deacetylases, or HDACs), which often leads to gene silencing typical of heterochromatin. Such heterochromatinization is initiated from a nucleation site and spreads bidirectionally until encountering boundaries that delimit the silenced areas. Recall from earlier in the text (see Chapter 4 ) the brief discussion of position effect, where repositioning of the \(w^{+}\) allele in Drosophila by translocation or inversion near heterochromatin produces intermittent \(w^{+}\) activity. In the heterozygous state \(\left(w^{+} / w\right),\) a variegated eye is produced, with white and red patches. How might one explain position-effect variegation in terms of histone acetylation and/or deacetylation?

An article entitled "Nucleosome Positioning at the Replication Fork" states: "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" (Lucchini et al., 2002). 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?

Supercoiled DNA is slightly unwound compared to relaxed DNA and this enables it to assume a more compact structure with enhanced physical stability. Describe the enzymes that control the number of supercoils present in the \(E .\) coli chromosome. How much would you have to reduce the linking number to increase the number of supercoils by five?

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