ets-l and ets-2 genes have previously been identified by their sequenc
e homology to the v-ets oncogene of the avian erythroblastosis virus,
E26. These cellular genes have been shown to function as transcription
factors important in lymphoid differentiation and activation and cell
ular proliferation. In this study, we have broadly analysed the differ
ential expression of ets-l and ets-2 during murine development using i
n situ hybridization. Our results indicate that these transcription fa
ctors are expressed in multiple tissues during critical stages of embr
yo formation and organogenesis, suggesting that these genes may serve
multiple functions during mouse development. The patterns of expressio
n of both genes are quite different as early as day 8.0 of gestation.
ets-l expression is clearly observed during a narrow developmental sta
ge in the developing nervous system, including the presumptive hindbra
in regions, the neural tube, as well as neural crest and the first and
second branchial arches. ets-2 expression is limited to the developin
g limb buds and distal tail. At later times, ets-l expression is obser
ved in developing vascular structures, including the heart, arteries,
capillaries and meninges, whereas ets-2 is highly expressed in develop
ing bone, tooth buds, epithelial layers of the gut, nasal sinus and ut
erus, and several regions of the developing brain. Both ets-l and ets-
2 are expressed in developing lung, gut and skin. High levels of expre
ssion in both genes is observed in adult lymphoid tissues, but in diff
erent tissue subsets. ets-l is expressed in the adult lung, gut mesenc
hyme and bone marrow. ets-2 continues to be expressed at low levels in
several adult tissues, except in the differentiated brain, where subs
tantial levels of expression are found in particular regions of the ma
ture brain. These results demonstrate that ets-l and ets-2 are differe
ntially regulated, are widely expressed in many tissues during murine
embryogenesis and may play important roles in cellular proliferation a
nd differentiation during mouse development.