Scholar Profile

David C. Page

Director, Whitehead Institute, Professor of Biology, Massachusetts Institute of Technology
Whitehead Institute
Massachusetts Institute of Technology
Nine Cambridge Center
Cambridge, MA 02142
Voice: 617-258-5203
Fax: 617-258-6505
Personal Homepage
1989 Searle Scholar
Former Member of Advisory Board (2014-2016)

Research Interests

Molecular Biology of Germline Determination and Gametogenesis

Germ cells occupy a central position in development, heredity, and evolution. In mammals, germ cells are first recognizable outside the portion of the embryo that will form the body. These primordial germ cells invade the developing body and migrate to the gonads, which at that stage are indistinguishable in males and females. The gonads differentiate into ovaries or testes. In parallel, the primordial germ cells become committed to give rise to oocytes or sperm. We use genetic tools to explore the development of the mammalian reproductive tract. While much of our research has focused on the mechanism by which the ovarian or testicular fate of the embryonic gonad is decided, our studies are increasingly directed toward understanding the mechanisms by which primordial germ cells give rise to gametes.

Germ Cell Development and Male Infertility: Three percent of men are infertile because of severe defects in sperm production. In few cases has the cause of spermatogenic failure been identified. We found that a particular portion of the Y chromosome is deleted de novo in 13% of men with no sperm in semen. These deletions define a region in which should be found one or more genes required for spermatogenesis (the Azoospermia Factor, AZF). These infertile men are otherwise healthy, suggesting that AZF is a "pure male sterile" locus. In the absence of AZF , spermatogenic output is diminished or extinguished, and in the more severe cases the testes contain no germ cells. We suspect that AZF may facilitate differentiation of primordial germ cells into spermatogonial stem cells or influence the destiny of these stem cells, which in normal males confront three alternative fates: proliferation, degeneration, or differentiation. The deletions encompass a gene, DAZ (Deleted in AZoospermia), which is expressed specifically in spermatogonia (and their immediate descendants, primary spermatocytes) and appears to encode an RNA binding protein. In Drosophila, a gene similar to DAZ is required for spermatogenesis. We are exploring the possibility that DAZ is AZF.

ZFX and ZFY: These genes, located on the X and Y chromosomes of all placental mammals, encode distinct but closely related proteins containing a highly acidic domain and 13 zinc fingers. The proteins likely function as sequence-specific activators of transcription. ZFY and ZFX were originally implicated in sex determination, but present evidence argues against such a role. Instead, our gene targeting experiments in mice suggest that ZFX contributes to early embryonic growth, animal size, and germ cell number in both males and females. Studies of these genes may also shed light on the evolution of X inactivation: while the mouse Zfx gene is X-inactivated, human ZFX is expressed on both "active" and "inactive" human X chromosomes.

Sex Determination: We are exploring mutations that cause gonadal sex reversal in humans or mice. By deletion studies of human XX males and XY females, we found that whether an embryo develops testes or ovaries is determined by the presence of less than 0.5% of the Y chromosome. SRY, a gene within this region, plays a pivotal role in gonadal sex determination. Other XY females, some human and some murine, appear to have intact Y chromosomes and are being studied for clues as to the identity of autosomal sex-determining genes operating upstream or downstream of SRY. In collaboration with Eva Eicher (Jackson Laboratory, Bar Harbor), we have carried out genetic linkage studies of XY sex reversal in mice. We have obtained evidence for and are presently localizing sex-determining genes on mouse chromosomes 2 and 4.

Turner Syndrome: Turner syndrome, classically associated with an XO karyotype, is a complex human phenotype of low viability in utero, short stature, ovarian failure, and somatic anatomic defects. Turner syndrome appears to be the result of monosomy for one or more genes common to the X and Y chromosomes. By deletion analysis, we identified a 100-kilobase-pair portion of the Y chromosome that probably contains one or more Turner genes. Within this region, we identified one gene, RPS4Y. A homolog on the X chromosome, RPS4X, escapes X inactivation. RPS4Y and RPS4X encode isoforms of ribosomal protein S4. Ribosomes from human male tissues contain both the X and Y-encoded protein isoforms, which are functionally interchangeable. We are testing the possibility that certain Turner features result from reduced protein synthetic capacity in embryos with only one RPS4 gene per cell.

Mapping and Cloning the Y Chromosome: A spectacular array of deletions, translocations, and other anomalies of the Y chromosome arise spontaneously in human populations. Using a battery of Y-DNA probes, we characterized aberrant Y chromosomes present in several hundred such individuals and constructed a 60-interval deletion map of the human Y chromosome. This map provides a foundation for studies of the Y's roles in germ cell development, sex determination, Turner syndrome, and tumorigenesis. We isolated virtually all of the euchromatic portion of the human Y chromosome, nearly 30 megabase-pairs of DNA overlapping YAC (yeast artificial chromosome) clones. We have embarked on an effort to dramatically refine the resolution of this map of overlapping clones and ordered, densely spaced markers.