PuSH - Publication Server of Helmholtz Zentrum München

Ebersole, T.A.* ; Ross, A.* ; Clark, E.* ; McGill, N.* ; Schindelhauer, D.* ; Cooke, H.* ; Grimes, B.*

Mammalian artificial chromosome formation from circular alphoid input DNA does not require telomere repeats.

Hum. Mol. Genet. 9, 1623-1631 (2000)
PMC
Open Access Green as soon as Postprint is submitted to ZB.
Mammalian artificial chromosomes (MACs) form in HT1080 cells after transfecting linear yeast artificial chromosome constructs minimally containing competent alphoid arrays, a selectable marker and terminal human telomere repeats. Restrictions on the structure of input DNA in MAC formation were investigated by transfecting circular or linear alphoid constructs with or without human telomere arrays and by varying the position and orientation of the telomere arrays on input linear constructs. Circular input DNA efficiently produced MACs. Absence of telomere arrays from circular input molecules did not significantly alter MAC formation rates. Linear constructs capped with telomere arrays generated MACs effectively, but a severe reduction in MAC formation was observed from linear constructs lacking telomere arrays. Human telomere arrays positioned 1-5 kb from linear construct ends and in either orientation were able to promote MAC formation with similar efficiencies. Both circular and linear input constructs generated artificial chromosomes that efficiently segregated in the absence of selection. Telomeres were not detected on the MACs, regardless of the inclusion of telomere arrays on input DNA, suggesting that circular chromosomes were formed. We found no evidence for acquisition of host cell DNA, which is consistent with de novo chromosome assembly.
Impact Factor
Scopus SNIP
Altmetric
0.000
0.000
Tags
Annotations
Special Publikation
Hide on homepage

Edit extra information
Edit own tags
Private
Edit own annotation
Private
Hide on publication lists
on hompage
Mark as special
publikation
Publication type Article: Journal article
Document type Scientific Article
Language english
Publication Year 2000
HGF-reported in Year 0
ISSN (print) / ISBN 0964-6906
e-ISSN 1460-2083
Quellenangaben Volume: 9, Issue: 11, Pages: 1623-1631 Article Number: , Supplement: ,
Publisher Oxford University Press
Reviewing status Peer reviewed
PubMed ID 10861289
Erfassungsdatum 2000-12-31