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Related Concept Videos

Lampbrush Chromosomes01:51

Lampbrush Chromosomes

In 1882, Flemming observed lampbrush chromosomes (LBC) in salamander eggs. Later in 1892, Rückert observed LBCs in shark egg cells and coined the term "lampbrush chromosomes" because they looked like brushes used to clean kerosene lamps.
LBCs are made up of two pairs of conjugating homologous chromatids. Each chromatid consists of alternatively positioned regions of condensed-inactive chromatin and loosely placed-active side loops, which can be contracted and extended. The loops resemble the...
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying DNA...
Polytene Chromosomes02:04

Polytene Chromosomes

Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also regularly...
Polytene Chromosomes02:04

Polytene Chromosomes

Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also regularly...
Heterochromatin02:38

Heterochromatin

The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at 9th...
Chromosome Duplication02:05

Chromosome Duplication

The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...

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Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
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Linearization of ancestral multichromosomal genomes.

Ján Maňuch1, Murray Patterson, Roland Wittler

  • 1INRIA Rhône-Alpes, 655 avenue de I'Europe, F-38344 Montbonnot, France. Murray.Patterson@inria.fr

BMC Bioinformatics
|January 4, 2013
PubMed
Summary

This study relaxes the Linearization Problem for ancestral genome reconstruction, making it solvable for genomes with multiple chromosomes. This breakthrough offers practical algorithms for complex genomic structures and aids in understanding linearization for ancestral genome inference.

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Area of Science:

  • Computational Biology
  • Bioinformatics
  • Genomics

Background:

  • Ancestral genome reconstruction often relies on binary matrices and the Consecutive-Ones Property (C1P).
  • The Linearization Problem, aiming to find maximum weight row subsets with C1P, is generally intractable for simple genome models (linear or single circular chromosome).

Purpose of the Study:

  • To explore a relaxed version of the Linearization Problem allowing for ancestral genomes with multiple linear or circular chromosomes.
  • To determine the computational complexity of this relaxed problem and establish tractability boundaries.

Main Methods:

  • Reduction of the relaxed Linearization Problem for binary matrices of degree two to a matching problem.
  • Analysis of complexity for matrices with row degrees 2 and 3 without multiplicity or weights.

Main Results:

  • The relaxed Linearization Problem is polynomially solvable for binary matrices of degree two (representing adjacencies), even with bounded column multiplicity (duplicated genes).
  • The problem becomes NP-complete for matrices with row degrees 2 and 3, without multiplicity and weights, defining sharp tractability limits.

Conclusions:

  • Relaxing the genome definition transforms an intractable problem into a tractable one, similar to the breakpoint median problem.
  • The developed algorithms are applicable to biological contexts like bacterial genomes with multiple replicons and can serve as heuristics for harder problem variants.
  • This research enhances the understanding of linearization techniques in ancestral genome structure inference.