home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
  HUM-MOLGEN -> Genetic News | search  

Birth Weight: Set And Match

  July, 2 2002 1:25
your information resource in human molecular genetics
Two independent pieces of research published in this week’s Nature (Vol. 417, No. 6892 27 June 2002) could explain why some babies are born small, and could also lend credence to evolutionary theories about the competition between male and female genes.

Babies with low birth weights are more likely to die as newborns and have an increased chance of physical or mental development problems. Low birth weight is also linked to an increased risk of coronary heart disease, type-2 diabetes and respiratory problems later in life.

Gordon Smith at the University of Cambridge, UK, and colleagues report in a Brief Communication (p. 916) that too little of a molecule associated with placenta development (called PAPP-A) produced during the first trimester of pregnancy may underlie low birth weight. This suggests that low birth weight may already have been determined by the time routine obstetric checks for this eventuality start, at 12 weeks.

Fetal growth may be controlled by a phenomenon called genetic imprinting, which controls expression of a fetus’s genes differently depending on whether the gene comes from the mother or father. The father contributes the gene that encodes insulin-like growth factor (IGF). More IGF means a big placenta that feeds more nutrients to the fetus. The result: a big, healthy baby that increases the chances of a male’s genes making it into the next generation. It is in the interests of the mother to combat the effect of this gene by expression of her own imprinted genes that control the size of her baby, preventing her from investing all her energy in one birth. This allows her to reproduce more than once so that as many of her genes as possible survive in subsequent generations.

Now Miguel Constancia and colleagues (pp. 945-948) have directly tested this conflict theory by specifically removing the IGF gene from the placenta of mice. This allowed contribution of male imprinted genes in the placenta to be analysed. They found that the mutants had a smaller placenta and reduced nutrient transport across it, leading to fetuses that are smaller than normal. Because the IGF gene is from the male, they provide the first evidence for the conflict theory in the placenta - the interface between mother and child.

It’s far too early to suggest that babies of low birth weight are the unwitting victims of a battle of the sexes, but the two studies provide clues to a potential mechanism and evolutionary explanation, argue Benjamin Tycko and Argiris Efstratiadis of Columbia University, New York, in an accompanying News and Views article.


Gordon C. S. Smith
tel +44 1223 76388
e-mail gcss2@cam.ac.uk

Miguel Constancia
tel +44 1223 496 301
e-mail Miguel.constancia@bbsrc.ac.uk

Benjamin Tycko
tel +1 212 304 7165
e-mail bt12@columbia.edu

Argiris Efstratiadis
tel +1 212 304 7159
e-mail arg@cancercenter.columbia.edu

(C) Nature press release.

Message posted by: Trevor M. D'Souza

print this article mail this article
Latest News
Variants Associated with Pediatric Allergic Disorder

Mutations in PHF6 Found in T-Cell Leukemia

Genetic Risk Variant for Urinary Bladder Cancer

Antibody Has Therapeutic Effect on Mice with ALS

Regulating P53 Activity in Cancer Cells

Anti-RNA Therapy Counters Breast Cancer Spread

Mitochondrial DNA Diversity

The Power of RNA Sequencing

‘Pro-Ageing' Therapy for Cancer?

Niche Genetics Influence Leukaemia

Molecular Biology: Clinical Promise for RNA Interference

Chemoprevention Cocktail for Colon Cancer

more news ...

Generated by News Editor 2.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995-2023 HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.