Genes regulating embryonic and fetal survival

被引:27
作者
Cross, JC [1 ]
机构
[1] Univ Calgary, Fac Med, Dept Biochem & Mol Biol, Calgary, AB T2N 4N1, Canada
关键词
embryo; cardiovascular; gene; implantation; placenta;
D O I
10.1016/S0093-691X(00)00454-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Embryonic mortality in both farm animals and humans occurs most frequently during the first few weeks after conception. It can be attributed to abnormalities in the earliest developmental processes during embryogenesis that include implantation, maternal recognition of pregnancy, and formation of the placenta and cardiovascular system. The molecular mechanisms that are essential for all of these early processes are being elucidated at a rapid pace using transgenic and gene knockout approaches in mice. Two important general conclusions have emerged from this work. First, placental defects can occur by a number of different molecular mechanisms and can result from defects in the development or function of its trophoblast, mesenchymal or vascular components. Second, placental and cardiovascular functions are intimately linked. Cells of the placenta, for example, produce hormones that have profound effects on maternal and fetal cardiac and vascular function. In addition, development of the two is linked mechanistically through the use of some genes that are essential for development of both. Understanding the molecular basis of these processes should help to address the major limits to the success of embryo transfer, IVF and embryo cloning practices in livestock species. (C) 2000 by Elsevier Science Inc.
引用
收藏
页码:193 / 207
页数:15
相关论文
共 92 条
[41]  
Ma GT, 1997, DEVELOPMENT, V124, P907
[42]   Genetic control of uterine receptivity during implantation [J].
Ma, L ;
Yao, ML ;
Maas, RL .
SEMINARS IN REPRODUCTIVE ENDOCRINOLOGY, 1999, 17 (03) :205-216
[43]   Reprogramming the cell cycle for endoreduplication in rodent trophoblast cells [J].
MacAuley, A ;
Cross, JC ;
Werb, Z .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (04) :795-807
[44]   ISOLATION OF A PLURIPOTENT CELL-LINE FROM EARLY MOUSE EMBRYOS CULTURED IN MEDIUM CONDITIONED BY TERATOCARCINOMA STEM-CELLS [J].
MARTIN, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (12) :7634-7638
[45]  
NAGY A, 1990, DEVELOPMENT, V110, P815
[46]   DERIVATION OF COMPLETELY CELL CULTURE-DERIVED MICE FROM EARLY-PASSAGE EMBRYONIC STEM-CELLS [J].
NAGY, A ;
ROSSANT, J ;
NAGY, R ;
ABRAMOWNEWERLY, W ;
RODER, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (18) :8424-8428
[47]   Placental expression and chromosomal localization of the human Gcm 1 gene [J].
Nait-Oumesmar, B ;
Copperman, AB ;
Lazzarini, RA .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (07) :915-922
[48]   Complementary tissue-specific expression of LIF and LIF-receptor mRNAs in early mouse embryogenesis [J].
Nichols, J ;
Davidson, D ;
Taga, T ;
Yoshida, K ;
Chambers, I ;
Smith, A .
MECHANISMS OF DEVELOPMENT, 1996, 57 (02) :123-131
[49]   Molecular pathways controlling heart development [J].
Olson, EN ;
Srivastava, D .
SCIENCE, 1996, 272 (5262) :671-676
[50]   INTERPLAY BETWEEN PROLIFERATION AND DIFFERENTIATION WITHIN THE MYOGENIC LINEAGE [J].
OLSON, EN .
DEVELOPMENTAL BIOLOGY, 1992, 154 (02) :261-272