[Home]
[Full version]
Loss of egg yolk genes in mammals and the origin of lactation and placentation
Mar 18 ,General Science
If you are reading this, you did not start your life by hatching from an egg. This is one of the many traits that you share with our mammalian relatives. A new paper in this week’s
PLoS Biology explores the genetic changes that led mammals to feed their young via the placenta and with milk, rather then via the egg, and finds that these changes occurred fairly gradually in our evolutionary history. The paper shows that milk-protein genes arose in a common ancestor of all existing mammalian lineages and preceded the loss of the genes that encoded egg proteins.
There are three living types of mammals: placental mammals (you, me, dogs, sheep, tigers, etc.), marsupial mammals (found in Australasia and South America, including kangaroos and possums), and monotremes (the duck-billed platypus and two species of Echidna).
The reproductive strategies of these three groups are very different. Placental mammals have long pregnancies and complicated placentas that provide nourishment to the embryo, followed by a relatively short period of lactation. Marsupials have a simpler form of placenta and much shorter pregnancies, followed by an extended period where the offspring is fed milk that changes in composition to meet the baby’s altering nutritional needs.
Monotremes—once a diverse group, but now restricted both in species number and distribution—have a much more reptilian beginning, as they lay eggs filled with yolk. While they do feed their young with milk, it is secreted onto a patch of skin rather then from a teat. How did these different strategies arise from our reptilian ancestors"
A new paper by David Brawand, Walter Wahli, and Henrik Kaessmann investigates the transition in offspring nutrition by comparing the genes of representatives of these three different mammalian lineages with those of the chicken—an egg-laying, milkless control. The authors found that there are similar genetic regions in all three mammalian lineages, suggesting that the genes for casein (a protein found in milk) arose in the mammalian common ancestor between 200 and 310 million years ago, prior to the evolution of the placenta.
Eggs contain a protein called vitellogenin as a major nutrient source. The authors looked for the genes associated with the production of vitellogenin, of which there are three in the chicken. They found that while monotremes still have one functional vitellogenin gene, in placental and marsupial mammals, all three have become pseudogenes (regions of the DNA that still closely resemble the functional gene, but which contain a few differences that have effectively turned the gene off). The gene-to-pseudogene transitions happened sequentially for the three genes, with the last one losing functionality 30-70 million years ago.
Therefore, mammals already had milk before they stopped laying eggs. Lactation reduced dependency on the egg as a source of nutrition for developing offspring, and the egg was abandoned completely in the marsupial and placental mammals in favor of the placenta. This meant that the genes associated with egg production gradually mutated, becoming pseudogenes, without affecting the fitness of the mammalian lineages.
Citation: Brawand D, Wahli W, Kaessmann H (2008) Loss of egg yolk genes in mammals and the origin of lactation and placentation. PLoS Biol 6(3): e63. doi:10.1371/journal.pbio.0060063
Source: Public Library of Science
Related stories:
Platypus genome explains animal's peculiar features; holds clues to evolution of mammals
The duck-billed platypus: part bird, part reptile, part mammal -- and the genome to prove it. An international consortium of scientists, led by Washington University School of Medicine in St. Louis, has decoded the genome of the platypus, showing that the animal's peculiar mix of features is reflected in its DNA. An analysis of the genome, published today in the journal
Nature, can help scientists piece together a more complete picture of the evolution of all mammals, including humans.
Discovery about fertilization points way to possible malaria vaccine
International investigations of an organism that one UT Southwestern Medical Center researcher calls a “silly little green scum” have led to key insights into the basic mechanisms of reproduction.
Antidepressant found to extend lifespan in C. elegans
A team of scientists led by Howard Hughes Medical Institute (HHMI) investigator Linda B. Buck has found that a drug used to treat depression can extend the lifespan of adult roundworms.
Researchers identify hundreds of genes controlling female fertility
Researchers at UT Southwestern Medical Center have found nearly 350 genes related to female fertility. Their research may open the door to much wider study in the poorly understood field of infertility.
Uni leads study on echidna sex life
A University of Adelaide-led project will study the genetic makeup of one of Australia's most iconic animals, the echidna, to give an unprecedented insight into their sex life and behaviour.
Rare Example of Darwinism Seen in Action
A research team of biologists has found experimental evidence that supports a controversial theory of genetic conflict in the reproduction of those animals that support their developing offspring through a placenta.
Scientists identify a mouse embryonic stem cell more like our own
Scientists have discovered a new type of mouse embryonic stem cell that is the closest counterpart yet to human embryonic stem (ES) cells, the National Institutes of Health (NIH) announced today. The cells are expected to serve as an improved model for human ES cells in studies of regeneration, disease pathology and basic stem cell biology.
Researchers replace organ in adult mice using 'single-parent' stem cells
Researchers at the University of Pennsylvania School of Veterinary Medicine have derived uniparental embryonic stem cells - created from a single donor's eggs or two sperm - and, for the first time, successfully used them to repopulate a damaged organ with healthy cells in adult mice. Their findings demonstrate that single-parent stem cells can proliferate normally in an adult organ and could provide a less controversial alternative to the therapeutic cloning of embryonic stem cells.
[Home]
[Full version]