{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T20:19:34Z","timestamp":1790194774246,"version":"4.1.0"},"reference-count":44,"publisher":"National Academy of Sciences","issue":"8","content-domain":{"domain":["www.pnas.org"],"crossmark-restriction":true},"short-container-title":["Proc. Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[2002,4,16]]},"abstract":"<jats:p>\n                    Pbx1 is a homeodomain protein that functions in complexes with other homeodomain-containing proteins to regulate gene expression during embryogenesis and oncogenesis. Pbx proteins bind DNA cooperatively as heterodimers or higher order complexes with Meis family members and Hox proteins and are believed to specify cell identity during development. Here, we present evidence that Pbx1, in partnership with Meis1b, can regulate posterior neural markers and neural crest marker genes during\n                    <jats:italic>Xenopus<\/jats:italic>\n                    development. A\n                    <jats:italic>Xenopus<\/jats:italic>\n                    homolog of the Pbx1b homeodomain protein was isolated and shown to be expressed throughout embryogenesis.\n                    <jats:italic>Xpbx1b<\/jats:italic>\n                    expression overlaps with\n                    <jats:italic>Xmeis1<\/jats:italic>\n                    in several areas, including the lateral neural folds, caudal branchial arch, hindbrain, and optic cup. When ectopically expressed, Xpbx1b can synergize with Xmeis1b to promote posterior neural and neural crest gene expression in ectodermal explants. Further, a physical interaction between these two homeodomain proteins is necessary for induction of these genes in embryonic tissue. In addition, coexpression of Xmeis1b and Xpbx1b leads to a prominent shift in the localization of Xmeis1b from the cytoplasm to the nucleus, suggesting that nuclear transport or retention of Xmeis1b may depend upon Xpbx1b. Finally, expression of a mutant construct in which Xpbx1b protein is fused to the repressor domain from\n                    <jats:italic>Drosophila<\/jats:italic>\n                    Engrailed inhibits posterior neural and neural crest gene expression. These data indicate that Xpbx1b and its partner, Xmeis1b, function in a transcriptional activation complex during hindbrain and neural crest development.\n                  <\/jats:p>","DOI":"10.1073\/pnas.082654899","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T10:45:09Z","timestamp":1027680309000},"page":"5448-5453","update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":44,"title":["<i>Xpbx1b<\/i>\n                    and\n                    <i>Xmeis1b<\/i>\n                    play a collaborative role in hindbrain and neural crest gene expression in\n                    <i>Xenopus<\/i>\n                    embryos"],"prefix":"10.1073","volume":"99","author":[{"given":"Ryu","family":"Maeda","sequence":"first","affiliation":[{"name":"Regulation of Cell Growth Laboratory, National Cancer Institute\u2013Frederick, Frederick, MD 21702; and Kimmel Cancer Center, Thomas Jefferson University, 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