Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1997-7-17
pubmed:abstractText
Previous studies indicated that members of the myc gene family may be essential for preimplantation development. Other studies revealed that preimplantation embryos lacking c-myc, N-myc, or L-myc are viable, indicating that these genes are either not essential for preimplantation development or can be substituted for functionally by other myc gene family members. To investigate the possible role of these genes during preimplantation development, we determined the temporal patterns of expression of four members of the myc gene family, genes encoding myc-associated proteins, and four putative MYC target genes. We observed a sequential pattern of myc gene expression, with the L-myc mRNA expressed as a maternal transcript, the c-myc mRNA expressed during the 4-cell through morula stages, and the B-myc mRNA expressed highly at the morula and blastocysts stages. B-myc was the predominant family member expressed during preimplantation development. The mxi mRNA was not detectable and the mad mRNA was detectable only as a maternal transcript. The max mRNA, however, was expressed both as a maternal mRNA and as an embryonic message throughout most of preimplantation development. Three putative MYC target genes (Odc, cyclin E, and prothymosin-alpha) were transcriptionally induced during the 2-cell stage, and their mRNAs increased sharply in abundance during development to the morula and blastocyst stages. Another putative MYC target gene, cyclin A, was expressed both as a maternal mRNA and as an embryonic transcript. These data support the view that the expression of myc target genes may be supported initially through the expression of maternally inherited MYC proteins and corresponding mRNAs and that subsequent stage-specific changes in expression of myc genes, myc-associated genes, and myc target genes may control early differentiative events around the time of implantation.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Amanitins, http://linkedlifedata.com/resource/pubmed/chemical/Basic Helix-Loop-Helix Leucine..., http://linkedlifedata.com/resource/pubmed/chemical/Basic-Leucine Zipper Transcription..., http://linkedlifedata.com/resource/pubmed/chemical/Chorionic Gonadotropin, http://linkedlifedata.com/resource/pubmed/chemical/Cyclins, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mad protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Max protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Myc associated factor X, http://linkedlifedata.com/resource/pubmed/chemical/Ornithine Decarboxylase, http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Thymosin, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/prothymosin alpha
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1040-452X
pubmed:author
pubmed:issnType
Print
pubmed:volume
47
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
57-65
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:9110315-Amanitins, pubmed-meshheading:9110315-Animals, pubmed-meshheading:9110315-Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, pubmed-meshheading:9110315-Basic-Leucine Zipper Transcription Factors, pubmed-meshheading:9110315-Blastocyst, pubmed-meshheading:9110315-Cell Differentiation, pubmed-meshheading:9110315-Chorionic Gonadotropin, pubmed-meshheading:9110315-Cyclins, pubmed-meshheading:9110315-DNA-Binding Proteins, pubmed-meshheading:9110315-Embryonic and Fetal Development, pubmed-meshheading:9110315-Female, pubmed-meshheading:9110315-Gene Expression Regulation, Developmental, pubmed-meshheading:9110315-Genes, myc, pubmed-meshheading:9110315-Male, pubmed-meshheading:9110315-Mice, pubmed-meshheading:9110315-Mice, Inbred Strains, pubmed-meshheading:9110315-Morula, pubmed-meshheading:9110315-Oocytes, pubmed-meshheading:9110315-Ornithine Decarboxylase, pubmed-meshheading:9110315-Protein Precursors, pubmed-meshheading:9110315-RNA, Messenger, pubmed-meshheading:9110315-Repressor Proteins, pubmed-meshheading:9110315-Thymosin, pubmed-meshheading:9110315-Transcription, Genetic, pubmed-meshheading:9110315-Transcription Factors
pubmed:year
1997
pubmed:articleTitle
Expression of myc-family, myc-interacting, and myc-target genes during preimplantation mouse development.
pubmed:affiliation
Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't