Telomere lengths at birth in trisomies 18 and 21 measured by Q-FISH
Trisomies 18 and 21 are genetic disorders in which cells possess an extra copy of each of the relevant chromosomes. Individuals with these disorders who survive birth generally have a shortened life expectancy. As telomeres are known to play an important role in the maintenance of genomic integrity...
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Published in | Gene Vol. 533; no. 1; pp. 199 - 207 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.01.2014
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Abstract | Trisomies 18 and 21 are genetic disorders in which cells possess an extra copy of each of the relevant chromosomes. Individuals with these disorders who survive birth generally have a shortened life expectancy. As telomeres are known to play an important role in the maintenance of genomic integrity by protecting the chromosomal ends, we conducted a study to determine whether there are differences in telomere length at birth between individuals with trisomy and diploidy, and between trisomic chromosomes and normal chromosomes. We examined samples of peripheral blood lymphocytes (PBLs) from 31 live neonates (diploidy: 10, trisomy 18: 10, trisomy 21: 11) and estimated the telomere length of each chromosome arm using Q-FISH. We observed that the telomeres of trisomic chromosomes were neither shorter nor longer than the mean telomere length of chromosomes as a whole among subjects with trisomies 18 and 21 (intra-cell comparison), and we were unable to conclude that there were differences in telomere length between 18 trisomy and diploid subjects, or between 21 trisomy and diploid subjects (inter-individual comparison). Although it has been reported that telomeres are shorter in older individuals with trisomy 21 and show accelerated telomere shortening with age, our data suggest that patients with trisomies 18 and 21 may have comparably sized telomeres. Therefore, it would be advisable for them to avoid lifestyle habits and characteristics such as obesity, cigarette smoking, chronic stress, and alcohol intake, which lead to marked telomere shortening.
•The first data of telomere length of 18 and 21 trisomy patients at chromosomal level•The telomere length in trisomies was not significantly shorter than that in controls.•The telomere lengths were very variable within the same cell, and individual at birth.•The telomere of the p-arm was longer than that of the q-arm in 32.3% of the subjects.•No specifically short telomeres on either arm of trisomic chromosomes at birth |
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AbstractList | Trisomies 18 and 21 are genetic disorders in which cells possess an extra copy of each of the relevant chromosomes. Individuals with these disorders who survive birth generally have a shortened life expectancy. As telomeres are known to play an important role in the maintenance of genomic integrity by protecting the chromosomal ends, we conducted a study to determine whether there are differences in telomere length at birth between individuals with trisomy and diploidy, and between trisomic chromosomes and normal chromosomes. We examined samples of peripheral blood lymphocytes (PBLs) from 31 live neonates (diploidy: 10, trisomy 18: 10, trisomy 21: 11) and estimated the telomere length of each chromosome arm using Q-FISH. We observed that the telomeres of trisomic chromosomes were neither shorter nor longer than the mean telomere length of chromosomes as a whole among subjects with trisomies 18 and 21 (intra-cell comparison), and we were unable to conclude that there were differences in telomere length between 18 trisomy and diploid subjects, or between 21 trisomy and diploid subjects (inter-individual comparison). Although it has been reported that telomeres are shorter in older individuals with trisomy 21 and show accelerated telomere shortening with age, our data suggest that patients with trisomies 18 and 21 may have comparably sized telomeres. Therefore, it would be advisable for them to avoid lifestyle habits and characteristics such as obesity, cigarette smoking, chronic stress, and alcohol intake, which lead to marked telomere shortening.
•The first data of telomere length of 18 and 21 trisomy patients at chromosomal level•The telomere length in trisomies was not significantly shorter than that in controls.•The telomere lengths were very variable within the same cell, and individual at birth.•The telomere of the p-arm was longer than that of the q-arm in 32.3% of the subjects.•No specifically short telomeres on either arm of trisomic chromosomes at birth Trisomies 18 and 21 are genetic disorders in which cells possess an extra copy of each of the relevant chromosomes. Individuals with these disorders who survive birth generally have a shortened life expectancy. As telomeres are known to play an important role in the maintenance of genomic integrity by protecting the chromosomal ends, we conducted a study to determine whether there are differences in telomere length at birth between individuals with trisomy and diploidy, and between trisomic chromosomes and normal chromosomes. We examined samples of peripheral blood lymphocytes (PBLs) from 31 live neonates (diploidy: 10, trisomy 18: 10, trisomy 21: 11) and estimated the telomere length of each chromosome arm using Q-FISH. We observed that the telomeres of trisomic chromosomes were neither shorter nor longer than the mean telomere length of chromosomes as a whole among subjects with trisomies 18 and 21 (intra-cell comparison), and we were unable to conclude that there were differences in telomere length between 18 trisomy and diploid subjects, or between 21 trisomy and diploid subjects (inter-individual comparison). Although it has been reported that telomeres are shorter in older individuals with trisomy 21 and show accelerated telomere shortening with age, our data suggest that patients with trisomies 18 and 21 may have comparably sized telomeres. Therefore, it would be advisable for them to avoid lifestyle habits and characteristics such as obesity, cigarette smoking, chronic stress, and alcohol intake, which lead to marked telomere shortening. Trisomies 18 and 21 are genetic disorders in which cells possess an extra copy of each of the relevant chromosomes. Individuals with these disorders who survive birth generally have a shortened life expectancy. As telomeres are known to play an important role in the maintenance of genomic integrity by protecting the chromosomal ends, we conducted a study to determine whether there are differences in telomere length at birth between individuals with trisomy and diploidy, and between trisomic chromosomes and normal chromosomes. We examined samples of peripheral blood lymphocytes (PBLs) from 31 live neonates (diploidy: 10, trisomy 18: 10, trisomy 21: 11) and estimated the telomere length of each chromosome arm using Q-FISH. We observed that the telomeres of trisomic chromosomes were neither shorter nor longer than the mean telomere length of chromosomes as a whole among subjects with trisomies 18 and 21 (intra-cell comparison), and we were unable to conclude that there were differences in telomere length between 18 trisomy and diploid subjects, or between 21 trisomy and diploid subjects (inter-individual comparison). Although it has been reported that telomeres are shorter in older individuals with trisomy 21 and show accelerated telomere shortening with age, our data suggest that patients with trisomies 18 and 21 may have comparably sized telomeres. Therefore, it would be advisable for them to avoid lifestyle habits and characteristics such as obesity, cigarette smoking, chronic stress, and alcohol intake, which lead to marked telomere shortening.Trisomies 18 and 21 are genetic disorders in which cells possess an extra copy of each of the relevant chromosomes. Individuals with these disorders who survive birth generally have a shortened life expectancy. As telomeres are known to play an important role in the maintenance of genomic integrity by protecting the chromosomal ends, we conducted a study to determine whether there are differences in telomere length at birth between individuals with trisomy and diploidy, and between trisomic chromosomes and normal chromosomes. We examined samples of peripheral blood lymphocytes (PBLs) from 31 live neonates (diploidy: 10, trisomy 18: 10, trisomy 21: 11) and estimated the telomere length of each chromosome arm using Q-FISH. We observed that the telomeres of trisomic chromosomes were neither shorter nor longer than the mean telomere length of chromosomes as a whole among subjects with trisomies 18 and 21 (intra-cell comparison), and we were unable to conclude that there were differences in telomere length between 18 trisomy and diploid subjects, or between 21 trisomy and diploid subjects (inter-individual comparison). Although it has been reported that telomeres are shorter in older individuals with trisomy 21 and show accelerated telomere shortening with age, our data suggest that patients with trisomies 18 and 21 may have comparably sized telomeres. Therefore, it would be advisable for them to avoid lifestyle habits and characteristics such as obesity, cigarette smoking, chronic stress, and alcohol intake, which lead to marked telomere shortening. |
Author | Poon, Steven S.S. Hiraishi, Naoki Fujiwara, Mutsunori Kawakami, Tadashi Ishikawa, Naoshi Nakao, Atsushi Nakamura, Ken-ichi Sawabe, Motoji Takubo, Kaiyo Izumiyama, Naotaka Aida, Junko Arai, Tomio Kuroiwa, Mie Matsuura, Masaaki |
Author_xml | – sequence: 1 givenname: Ken-ichi surname: Nakamura fullname: Nakamura, Ken-ichi email: cpn@tmig.or.jp organization: Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan – sequence: 2 givenname: Naoshi surname: Ishikawa fullname: Ishikawa, Naoshi email: naoshi@tmig.or.jp organization: Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan – sequence: 3 givenname: Naotaka surname: Izumiyama fullname: Izumiyama, Naotaka organization: Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan – sequence: 4 givenname: Junko surname: Aida fullname: Aida, Junko organization: Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan – sequence: 5 givenname: Mie surname: Kuroiwa fullname: Kuroiwa, Mie organization: Department of Pathophysiology, Yokohama College of Pharmacy, Yokohama 245-0066, Japan – sequence: 6 givenname: Naoki surname: Hiraishi fullname: Hiraishi, Naoki organization: Department of Laboratory Medicine, Hadano Red Cross Hospital, Hadano, Kanagawaken 257-0017, Japan – sequence: 7 givenname: Mutsunori surname: Fujiwara fullname: Fujiwara, Mutsunori organization: Department of Pathology and Laboratory Medicine, Japanese Red Cross Medical Center, Tokyo, Japan – sequence: 8 givenname: Atsushi surname: Nakao fullname: Nakao, Atsushi organization: Department of Neonatal Medicine, Japanese Red Cross Medical Center, Tokyo, Japan – sequence: 9 givenname: Tadashi surname: Kawakami fullname: Kawakami, Tadashi organization: Department of Neonatal Medicine, Japanese Red Cross Medical Center, Tokyo, Japan – sequence: 10 givenname: Steven S.S. surname: Poon fullname: Poon, Steven S.S. organization: Terry Fox Laboratory, British Columbia Cancer Research Centre, Vancouver, BC, Canada – sequence: 11 givenname: Masaaki surname: Matsuura fullname: Matsuura, Masaaki organization: Bioinformatics Group, Genome Center and Department of Cancer Genomics, The Cancer Institute, The Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan – sequence: 12 givenname: Motoji surname: Sawabe fullname: Sawabe, Motoji organization: Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo 173-0015, Japan – sequence: 13 givenname: Tomio surname: Arai fullname: Arai, Tomio organization: Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo 173-0015, Japan – sequence: 14 givenname: Kaiyo surname: Takubo fullname: Takubo, Kaiyo email: takubo@tmig.or.jp organization: Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan |
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Keywords | TFU PNA Q-FISH Trisomy 18 TRF DAPI Down syndrome Telomere Telo C Trisomy 21 kbp PDL PBL CENP1 quantitative fluorescence in situ hybridization population doubling level FITC-labeled CTTCGTTGGAAACGGGGT peptide nucleic acid probe kilobase pairs terminal restriction fragment telomere fluorescence unit peripheral blood lymphocyte 4′, 6-diamidino-2-phenylindole Cy3-labeled (CCCTAA)3 peptide nucleic acid probe peptide nucleic acid |
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Snippet | Trisomies 18 and 21 are genetic disorders in which cells possess an extra copy of each of the relevant chromosomes. Individuals with these disorders who... |
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SubjectTerms | alcohol drinking Calibration Chromosomes, Human, Pair 18 Diploidy Down syndrome Down Syndrome - genetics genetic disorders Humans In Situ Hybridization, Fluorescence - methods Infant, Newborn Karyotyping lifestyle longevity lymphocytes neonates obesity patients Q-FISH smoking (habit) Telomere telomeres trisomics Trisomy Trisomy 18 Trisomy 21 |
Title | Telomere lengths at birth in trisomies 18 and 21 measured by Q-FISH |
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