Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies

Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood....
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Autor*in:	Sharakhov, Igor V [verfasserIn] Artemov, Gleb N Sharakhova, Maria V

Format:	Artikel
Sprache:	Englisch

Erschienen:	2016

Rechteinformationen:	Nutzungsrecht: © 2016, World Scientific Publishing Company

Übergeordnetes Werk:	Enthalten in: Journal of bioinformatics and computational biology - Londorn : Imperial College Press, 2003, 14(2016), 2
Übergeordnetes Werk:	volume:14 ; year:2016 ; number:2

Links:	Volltext

DOI / URN:	10.1142/S0219720016300033

Katalog-ID:	OLC197620559X

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520			\|a Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements.
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allfields	10.1142/S0219720016300033 doi PQ20160610 (DE-627)OLC197620559X (DE-599)GBVOLC197620559X (PRQ)worldscientific_primary_S02197200163000330 (KEY)0519760020160000014000200000chromosomeevolutioninmalariamosquitoesinferredfrom DE-627 ger DE-627 rakwb eng 570 ZDB 42.11 bkl 42.13 bkl 54.80 bkl Sharakhov, Igor V verfasserin aut Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements. Nutzungsrecht: © 2016, World Scientific Publishing Company Artemov, Gleb N oth Sharakhova, Maria V oth Enthalten in Journal of bioinformatics and computational biology Londorn : Imperial College Press, 2003 14(2016), 2 (DE-627)37660753X (DE-600)2131422-6 (DE-576)45226524X 0219-7200 nnns volume:14 year:2016 number:2 http://dx.doi.org/10.1142/S0219720016300033 Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-MAT SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2190 42.11 AVZ 42.13 AVZ 54.80 AVZ AR 14 2016 2
spelling	10.1142/S0219720016300033 doi PQ20160610 (DE-627)OLC197620559X (DE-599)GBVOLC197620559X (PRQ)worldscientific_primary_S02197200163000330 (KEY)0519760020160000014000200000chromosomeevolutioninmalariamosquitoesinferredfrom DE-627 ger DE-627 rakwb eng 570 ZDB 42.11 bkl 42.13 bkl 54.80 bkl Sharakhov, Igor V verfasserin aut Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements. Nutzungsrecht: © 2016, World Scientific Publishing Company Artemov, Gleb N oth Sharakhova, Maria V oth Enthalten in Journal of bioinformatics and computational biology Londorn : Imperial College Press, 2003 14(2016), 2 (DE-627)37660753X (DE-600)2131422-6 (DE-576)45226524X 0219-7200 nnns volume:14 year:2016 number:2 http://dx.doi.org/10.1142/S0219720016300033 Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-MAT SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2190 42.11 AVZ 42.13 AVZ 54.80 AVZ AR 14 2016 2
allfields_unstemmed	10.1142/S0219720016300033 doi PQ20160610 (DE-627)OLC197620559X (DE-599)GBVOLC197620559X (PRQ)worldscientific_primary_S02197200163000330 (KEY)0519760020160000014000200000chromosomeevolutioninmalariamosquitoesinferredfrom DE-627 ger DE-627 rakwb eng 570 ZDB 42.11 bkl 42.13 bkl 54.80 bkl Sharakhov, Igor V verfasserin aut Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements. Nutzungsrecht: © 2016, World Scientific Publishing Company Artemov, Gleb N oth Sharakhova, Maria V oth Enthalten in Journal of bioinformatics and computational biology Londorn : Imperial College Press, 2003 14(2016), 2 (DE-627)37660753X (DE-600)2131422-6 (DE-576)45226524X 0219-7200 nnns volume:14 year:2016 number:2 http://dx.doi.org/10.1142/S0219720016300033 Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-MAT SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2190 42.11 AVZ 42.13 AVZ 54.80 AVZ AR 14 2016 2
allfieldsGer	10.1142/S0219720016300033 doi PQ20160610 (DE-627)OLC197620559X (DE-599)GBVOLC197620559X (PRQ)worldscientific_primary_S02197200163000330 (KEY)0519760020160000014000200000chromosomeevolutioninmalariamosquitoesinferredfrom DE-627 ger DE-627 rakwb eng 570 ZDB 42.11 bkl 42.13 bkl 54.80 bkl Sharakhov, Igor V verfasserin aut Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements. Nutzungsrecht: © 2016, World Scientific Publishing Company Artemov, Gleb N oth Sharakhova, Maria V oth Enthalten in Journal of bioinformatics and computational biology Londorn : Imperial College Press, 2003 14(2016), 2 (DE-627)37660753X (DE-600)2131422-6 (DE-576)45226524X 0219-7200 nnns volume:14 year:2016 number:2 http://dx.doi.org/10.1142/S0219720016300033 Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-MAT SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2190 42.11 AVZ 42.13 AVZ 54.80 AVZ AR 14 2016 2
allfieldsSound	10.1142/S0219720016300033 doi PQ20160610 (DE-627)OLC197620559X (DE-599)GBVOLC197620559X (PRQ)worldscientific_primary_S02197200163000330 (KEY)0519760020160000014000200000chromosomeevolutioninmalariamosquitoesinferredfrom DE-627 ger DE-627 rakwb eng 570 ZDB 42.11 bkl 42.13 bkl 54.80 bkl Sharakhov, Igor V verfasserin aut Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements. Nutzungsrecht: © 2016, World Scientific Publishing Company Artemov, Gleb N oth Sharakhova, Maria V oth Enthalten in Journal of bioinformatics and computational biology Londorn : Imperial College Press, 2003 14(2016), 2 (DE-627)37660753X (DE-600)2131422-6 (DE-576)45226524X 0219-7200 nnns volume:14 year:2016 number:2 http://dx.doi.org/10.1142/S0219720016300033 Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-MAT SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_70 GBV_ILN_2190 42.11 AVZ 42.13 AVZ 54.80 AVZ AR 14 2016 2
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title_sort	chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies
title_auth	Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies
abstract	Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements.
abstractGer	Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements.
abstract_unstemmed	Polymorphic inversions in mosquitoes are distributed nonrandomly among chromosomes and are associated with ecological, behavioral, and physiological adaptations related to pathogen transmission. Despite their significance, the patterns and mechanism of genome rearrangements are not well understood. Recent sequencing and physical mapping of the genomes for 16 Anopheles mosquito species provided an opportunity to study chromosome evolution at the highest resolution. New studies revealed that fixed rearrangement accumulated ∼ 3 times faster on the X chromosome than on autosomes. The highest densities of transposable elements (TEs) and satellites of different sizes have also been found on the X chromosome, suggesting a mechanism for the inversion generation. The high rate of X chromosome rearrangements is in sharp contrast with the paucity of polymorphic inversions on the X in the majority of anopheline species. This paper highlights the advances in understanding chromosome evolution in malaria vectors and discusses possible future directions in studying mechanisms and biological roles of genome rearrangements.
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title_short	Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies
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Chromosome evolution in malaria mosquitoes inferred from physically mapped genome assemblies

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