Literature DB >> 8115596

Genetic conflicts in human pregnancy.

D Haig1.   

Abstract

Pregnancy has commonly been viewed as a cooperative interaction between a mother and her fetus. The effects of natural selection on genes expressed in fetuses, however, may be opposed by the effects of natural selection on genes expressed in mothers. In this sense, a genetic conflict can be said to exist between maternal and fetal genes. Fetal genes will be selected to increase the transfer of nutrients to their fetus, and maternal genes will be selected to limit transfers in excess of some maternal optimum. Thus a process of evolutionary escalation is predicted in which fetal actions are opposed by maternal countermeasures. The phenomenon of genomic imprinting means that a similar conflict exists within fetal cells between genes that are expressed when maternally derived, and genes that are expressed when paternally derived. During implantation, fetally derived cells (trophoblast) invade the maternal endometrium and remodel the endometrial spiral arteries into low-resistance vessels that are unable to constrict. This invasion has three consequences. First, the fetus gains direct access to its mother's arterial blood. Therefore, a mother cannot reduce the nutrient content of blood reaching the placenta without reducing the nutrient supply to her own tissues. Second, the volume of blood reaching the placenta becomes largely independent of control by the local maternal vasculature. Third, the placenta is able to release hormones and other substances directly into the maternal circulation. Placental hormones, including human chorionic gonadotropin (hCG) and human placental lactogen (hPL), are predicted to manipulate maternal physiology for fetal benefit. For example, hPL is proposed to act on maternal prolactin receptors to increase maternal resistance to insulin. If unopposed, the effect of hPL would be to maintain higher blood glucose levels for longer periods after meals. This action, however, is countered by increased maternal production of insulin. Gestational diabetes develops if the mother is unable to mount an adequate response to fetal manipulation. Similarly, fetal genes are predicted to enhance the flow of maternal blood through the placenta by increasing maternal blood pressure. Preeclampsia can be interpreted as an attempt by a poorly nourished fetus to increase its supply of nutrients by increasing the resistance of its mother's peripheral circulation.

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Year:  1993        PMID: 8115596     DOI: 10.1086/418300

Source DB:  PubMed          Journal:  Q Rev Biol        ISSN: 0033-5770            Impact factor:   4.875


  183 in total

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Authors:  J H Werren; M J Hatcher
Journal:  Genetics       Date:  2000-07       Impact factor: 4.562

Review 2.  On the difficulty of defining disease: a Darwinian perspective.

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Review 3.  Pathophysiology and maternal biologic markers of preeclampsia.

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6.  Defining the function of a prolactin gene family member.

Authors:  Jonathan A Green
Journal:  Proc Natl Acad Sci U S A       Date:  2004-11-16       Impact factor: 11.205

7.  Retroviruses push the envelope for mammalian placentation.

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Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-26       Impact factor: 11.205

8.  Alternatives to the grandmother hypothesis: a meta-analysis of the association between grandparental and grandchild survival in patrilineal populations.

Authors:  Beverly I Strassmann; Wendy M Garrard
Journal:  Hum Nat       Date:  2011-07

9.  Molecular and vascular targets in the pathogenesis and management of the hypertension associated with preeclampsia.

Authors:  Ossama M Reslan; Raouf A Khalil
Journal:  Cardiovasc Hematol Agents Med Chem       Date:  2010-10-01

10.  Life history consequences of mammal sibling rivalry.

Authors:  P Stockley; G A Parker
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-17       Impact factor: 11.205

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