Home LiteratureArticle Details
PMID: 6724137 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Studies of the temporal relationship between the cytogenetic and biochemical manifestations of X-chromosome inactivation during the differentiation of LT-1 teratocarcinoma stem cells.

Developmental biology ·Vol. 103 ·No. 2 ·1984-06-00 ·Pages 425-33

Takagi N, Martin GR

Abstract

Previous biochemical studies have suggested that both X chromosomes produce gene products when cells of the LT-1 teratocarcinoma stem cell line are maintained in the undifferentiated state, and that dosage compensation, the biochemical manifestation of X inactivation, occurs when the cells are induced to differentiate in vitro (Martin et al., 1978). In this study the differentiation of LT-1 cells in vitro is described in detail, and data from cytogenetic studies of the time of X-chromosome replication in LT-1 cells are presented. They show that as long as the cells are maintained in the undifferentiated state both X chromosomes in each cell show the isocyclic replication pattern typical of a genetically active chromosome. However, when the LT-1 cells are induced to differentiate under appropriate conditions, one of the two X chromosomes in each cell of a large proportion of the population displays the allocyclic (either early or late) replication pattern typical of an inactive X chromosome. These data thus confirm that undifferentiated LT-1 cells contain two active X chromosomes and that X inactivation occurs in differentiating cultures of LT-1 cells. It is further demonstrated that there is a close temporal correlation between the biochemical and cytogenetic manifestations of the X-inactivation process. In addition, we observed that although X inactivation does not occur in the absence of morphological differentiation, it does not always occur when the cells differentiate in vitro.

MeSH Terms
Animals Bromodeoxyuridine Cell Differentiation Cell Line Chromosome Banding DNA Replication Dosage Compensation, Genetic Endoderm/cytology Female Glucosephosphate Dehydrogenase/metabolism Metaphase Mice Microscopy, Fluorescence Phosphogluconate Dehydrogenase/metabolism Stem Cells/cytology Teratoma/genetics,pathology,physiopathology Time Factors X Chromosome/metabolism
Chemicals
Phosphogluconate Dehydrogenase Glucosephosphate Dehydrogenase Bromodeoxyuridine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Takagi N
Martin G R
Article Info
Journal
Developmental biology
Abbr.
Dev Biol
ISSN
0012-1606
Published
1984-06-00
Pages
425-33
Language
English
Region
United States
NLM ID
0372762
Subset
IM
Grants
NCI NIH HHS · R01 CA25966 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]