Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Integration of fluorescence in situ hybridization and chromosome-length genome assemblies revealed synteny map for guinea pig, naked mole-rat, and human. / Romanenko, Svetlana A; Kliver, Sergei F; Serdyukova, Natalia A и др.
в: Scientific Reports, Том 13, № 1, 21055, 29.11.2023.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
}
TY - JOUR
T1 - Integration of fluorescence in situ hybridization and chromosome-length genome assemblies revealed synteny map for guinea pig, naked mole-rat, and human
AU - Romanenko, Svetlana A
AU - Kliver, Sergei F
AU - Serdyukova, Natalia A
AU - Perelman, Polina L
AU - Trifonov, Vladimir A
AU - Seluanov, Andrei
AU - Gorbunova, Vera
AU - Azpurua, Jorge
AU - Pereira, Jorge C
AU - Ferguson-Smith, Malcolm A
AU - Graphodatsky, Alexander S
N1 - VG and AS are supported by grants from the US National Institutes of Health. This research was funded by Russian Science Foundation grant No 19-14-00034-П (ASG). The research was completed using equipment (materials) of the Core Facilities Centre “Cryobank of cell cultures” Institute of Molecular and Cellular Biology SB RAS (Novosibirsk, Russia). © 2023. The Author(s). Публикация для корректировки.
PY - 2023/11/29
Y1 - 2023/11/29
N2 - Descriptions of karyotypes of many animal species are currently available. In addition, there has been a significant increase in the number of sequenced genomes and an ever-improving quality of genome assembly. To close the gap between genomic and cytogenetic data we applied fluorescent in situ hybridization (FISH) and Hi-C technology to make the first full chromosome-level genome comparison of the guinea pig (Cavia porcellus), naked mole-rat (Heterocephalus glaber), and human. Comparative chromosome maps obtained by FISH with chromosome-specific probes link genomic scaffolds to individual chromosomes and orient them relative to centromeres and heterochromatic blocks. Hi-C assembly made it possible to close all gaps on the comparative maps and to reveal additional rearrangements that distinguish the karyotypes of the three species. As a result, we integrated the bioinformatic and cytogenetic data and adjusted the previous comparative maps and genome assemblies of the guinea pig, naked mole-rat, and human. Syntenic associations in the two hystricomorphs indicate features of their putative ancestral karyotype. We postulate that the two approaches applied in this study complement one another and provide complete information about the organization of these genomes at the chromosome level.
AB - Descriptions of karyotypes of many animal species are currently available. In addition, there has been a significant increase in the number of sequenced genomes and an ever-improving quality of genome assembly. To close the gap between genomic and cytogenetic data we applied fluorescent in situ hybridization (FISH) and Hi-C technology to make the first full chromosome-level genome comparison of the guinea pig (Cavia porcellus), naked mole-rat (Heterocephalus glaber), and human. Comparative chromosome maps obtained by FISH with chromosome-specific probes link genomic scaffolds to individual chromosomes and orient them relative to centromeres and heterochromatic blocks. Hi-C assembly made it possible to close all gaps on the comparative maps and to reveal additional rearrangements that distinguish the karyotypes of the three species. As a result, we integrated the bioinformatic and cytogenetic data and adjusted the previous comparative maps and genome assemblies of the guinea pig, naked mole-rat, and human. Syntenic associations in the two hystricomorphs indicate features of their putative ancestral karyotype. We postulate that the two approaches applied in this study complement one another and provide complete information about the organization of these genomes at the chromosome level.
KW - Humans
KW - Guinea Pigs
KW - Animals
KW - Synteny
KW - In Situ Hybridization, Fluorescence
KW - Genome
KW - Karyotype
KW - Mole Rats/genetics
U2 - 10.1038/s41598-023-46595-x
DO - 10.1038/s41598-023-46595-x
M3 - Article
C2 - 38030702
VL - 13
JO - Scientific Reports
JF - Scientific Reports
SN - 2045-2322
IS - 1
M1 - 21055
ER -
ID: 59287394