Wolf Reik: Inheritance beyond DNA

نویسنده

  • Nicole LeBrasseur
چکیده

F or all it has given to science, Mendelian genetics is now a sim-plistic view of inheritance. On top of the DNA code lies another genetic " language, " the epigenetic code. Wolf Reik has built a career of decoding this language. Reik jumped on the now crowded epigenetic bandwagon when it was in its infancy, during both his PhD with Rudolf Jaenisch in Germany and his postdoc with Azim Surani in the UK. At the Babraham Institute, where he's been for 15 years now, Reik has delved into the molecular aspects of epigenetics and its role in imprinting (1)—the developmental control of gene expression based on a gene's maternal vs. paternal origin. His group has discovered that imprinting is controlled both by noncoding RNAs (2) and by the three-dimensional arrangement of chromatin (3). Along the way, Reik and colleagues have uncovered functions for imprinted genes in fetal growth (4). The Reik laboratory is now examining developmental changes in epigenetic marks as cell fates are established (5). They are also interested in how the widespread erasure of epi-genetic information may help reset pluripotency in germ cells or in the zygote, for example (6). In a recent conversation , Reik confessed to daydreams of a clinical practice while he focuses on the basic mechanisms behind epige-netic reprogramming. That reverie, he explains, is sated by collaborative projects that bring together his molecular studies and epigenetics-related human disorders. How did you end up in a scientifi c career? I guess partly because both of my parents are scientists. [laughs] We were exposed to a scientifi c kind of thinking throughout our lives. As a teenager I was interested in many different things, including literature and music. Studying medicine at that time kept a number of my options open. At university in Germany, I did several clinical stints, which I really enjoyed. I also worked in a country hospital in Brazil, which was both interesting and rewarding. It showed me that you can really help people even with quite limited technology. How, then, did you come to pursue research rather than a clinical practice? It was always lurking in the back of my mind that I might enjoy research. Then I went to a seminar by Rudolf Jaenisch; he's a very good speaker, and he can enthuse people. I thought, " Wow, there's a world there that I don't know about. " The next …

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Reprogramming the Methylome: Erasing Memory and Creating Diversity

The inheritance of epigenetic marks, in particular DNA methylation, provides a molecular memory that ensures faithful commitment to transcriptional programs during mammalian development. Epigenetic reprogramming results in global hypomethylation of the genome together with a profound loss of memory, which underlies naive pluripotency. Such global reprogramming occurs in primordial germ cells, e...

متن کامل

Epigenetic reprogramming in plant and animal development.

Epigenetic modifications of the genome are generally stable in somatic cells of multicellular organisms. In germ cells and early embryos, however, epigenetic reprogramming occurs on a genome-wide scale, which includes demethylation of DNA and remodeling of histones and their modifications. The mechanisms of genome-wide erasure of DNA methylation, which involve modifications to 5-methylcytosine ...

متن کامل

Epigenetic inheritance in the mouse

Acquired epigenetic modifications, such as DNA methylation or stable chromatin structures, are not normally thought to be inherited through the germline to future generations in mammals [1] [2]. Studies in the mouse have shown that specific manipulations of early embryos, such as nuclear transplantation, can result in altered patterns of gene expression and induce phenotypic alterations at late...

متن کامل

Dna Demethylation by Dna Repair Accessed Terms of Use Detailed Terms

Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters.

متن کامل

parental origin effect in Huntington's chorea

Huntington's disease (HD) is an autosomal dominant condition with almost complete penetrance. The age of onset of the symptoms, however, is variable and depends on the parental origin of the gene. A high proportion of early onset cases inherit the HD gene from their father, whereas a considerable proportion of late onset cases inherit the gene from their mother. Modification of the HD gene by m...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 188  شماره 

صفحات  -

تاریخ انتشار 2010