Matches in SemOpenAlex for { <https://semopenalex.org/work/W3173194772> ?p ?o ?g. }
- W3173194772 endingPage "204" @default.
- W3173194772 startingPage "183" @default.
- W3173194772 abstract "The mechanisms regulating nervous system development are still unknown for a wide variety of taxa. In insects and vertebrates, bone morphogenetic protein (BMP) signaling plays a key role in establishing the dorsal-ventral (D-V) axis and limiting the neuroectoderm to one side of that axis, leading to speculation about the conserved evolution of centralized nervous systems. Studies outside of insects and vertebrates show a more diverse picture of what, if any role, BMP signaling plays in neural development across Bilateria. This is especially true in the morphologically diverse Spiralia (≈Lophotrochozoa). Despite several studies of D-V axis formation and neural induction in spiralians, there is no consensus for how these two processes are related, or whether BMP signaling may have played an ancestral role in either process. To determine the function of BMP signaling during early development of the spiralian annelid Capitella teleta, we incubated embryos and larvae in BMP4 protein for different amounts of time. Adding exogenous BMP protein to early-cleaving C. teleta embryos had a striking effect on formation of the brain, eyes, foregut, and ventral midline in a time-dependent manner. However, adding BMP did not block brain or VNC formation or majorly disrupt the D-V axis. We identified three key time windows of BMP activity. 1) BMP treatment around birth of the 3rd-quartet micromeres caused the loss of the eyes, radialization of the brain, and a reduction of the foregut, which we interpret as a loss of A- and C-quadrant identities with a possible trans-fate switch to a D-quadrant identity. 2) Treatment after the birth of micromere 4d induced formation of a third ectopic brain lobe, eye, and foregut lobe, which we interpret as a trans-fate switch of B-quadrant micromeres to a C-quadrant identity. 3) Continuous BMP treatment from late cleavage (4d + 12 h) through mid-larval stages resulted in a modest expansion of Ct-chrdl expression in the dorsal ectoderm and a concomitant loss of the ventral midline (neurotroch ciliary band). Loss of the ventral midline was accompanied by a collapse of the bilaterally-symmetric ventral nerve cord, although the total amount of neural tissue was not greatly affected. Our results compared with those from other annelids and molluscs suggest that BMP signaling was not ancestrally involved in delimiting neural tissue to one region of the D-V axis. However, the effects of ectopic BMP on quadrant-identity during cleavage stages may represent a non-axial organizing signal that was present in the last common ancestor of annelids and mollusks. Furthermore, in the last common ancestor of annelids, BMP signaling may have functioned in patterning ectodermal fates along the D-V axis in the trunk. Ultimately, studies on a wider range of spiralian taxa are needed to determine the role of BMP signaling during neural induction and neural patterning in the last common ancestor of this group. Ultimately, these comparisons will give us insight into the evolutionary origins of centralized nervous systems and body plans." @default.
- W3173194772 created "2021-07-05" @default.
- W3173194772 creator A5018696818 @default.
- W3173194772 creator A5037763610 @default.
- W3173194772 creator A5044828935 @default.
- W3173194772 creator A5091538795 @default.
- W3173194772 date "2021-10-01" @default.
- W3173194772 modified "2023-10-11" @default.
- W3173194772 title "Role of BMP signaling during early development of the annelid Capitella teleta" @default.
- W3173194772 cites W1496387202 @default.
- W3173194772 cites W1513068949 @default.
- W3173194772 cites W1545639216 @default.
- W3173194772 cites W1552332385 @default.
- W3173194772 cites W1599136426 @default.
- W3173194772 cites W1663371441 @default.
- W3173194772 cites W1985434562 @default.
- W3173194772 cites W1989966533 @default.
- W3173194772 cites W1990982364 @default.
- W3173194772 cites W2011175428 @default.
- W3173194772 cites W2015886976 @default.
- W3173194772 cites W2019124119 @default.
- W3173194772 cites W2021100834 @default.
- W3173194772 cites W2023265934 @default.
- W3173194772 cites W2024610606 @default.
- W3173194772 cites W2026579464 @default.
- W3173194772 cites W2028141052 @default.
- W3173194772 cites W2035891406 @default.
- W3173194772 cites W2040203559 @default.
- W3173194772 cites W2047642636 @default.
- W3173194772 cites W2054516370 @default.
- W3173194772 cites W2067144256 @default.
- W3173194772 cites W2072923797 @default.
- W3173194772 cites W2073857918 @default.
- W3173194772 cites W2075478382 @default.
- W3173194772 cites W2078805618 @default.
- W3173194772 cites W2091734168 @default.
- W3173194772 cites W2097923096 @default.
- W3173194772 cites W2117484859 @default.
- W3173194772 cites W2117862746 @default.
- W3173194772 cites W2134436946 @default.
- W3173194772 cites W2140746618 @default.
- W3173194772 cites W2155253806 @default.
- W3173194772 cites W2158295165 @default.
- W3173194772 cites W2163031867 @default.
- W3173194772 cites W2167279371 @default.
- W3173194772 cites W2187557086 @default.
- W3173194772 cites W2200431692 @default.
- W3173194772 cites W2281524121 @default.
- W3173194772 cites W2461141759 @default.
- W3173194772 cites W2521767182 @default.
- W3173194772 cites W2560368704 @default.
- W3173194772 cites W2580035316 @default.
- W3173194772 cites W2739972158 @default.
- W3173194772 cites W2750748793 @default.
- W3173194772 cites W2757747635 @default.
- W3173194772 cites W2762801938 @default.
- W3173194772 cites W2774307240 @default.
- W3173194772 cites W2784288021 @default.
- W3173194772 cites W2797062146 @default.
- W3173194772 cites W2810352840 @default.
- W3173194772 cites W2892595819 @default.
- W3173194772 cites W2905809473 @default.
- W3173194772 cites W3042940930 @default.
- W3173194772 cites W3048603339 @default.
- W3173194772 cites W3087848821 @default.
- W3173194772 cites W3141182766 @default.
- W3173194772 cites W4244540455 @default.
- W3173194772 doi "https://doi.org/10.1016/j.ydbio.2021.06.011" @default.
- W3173194772 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34216573" @default.
- W3173194772 hasPublicationYear "2021" @default.
- W3173194772 type Work @default.
- W3173194772 sameAs 3173194772 @default.
- W3173194772 citedByCount "6" @default.
- W3173194772 countsByYear W31731947722021 @default.
- W3173194772 countsByYear W31731947722022 @default.
- W3173194772 countsByYear W31731947722023 @default.
- W3173194772 crossrefType "journal-article" @default.
- W3173194772 hasAuthorship W3173194772A5018696818 @default.
- W3173194772 hasAuthorship W3173194772A5037763610 @default.
- W3173194772 hasAuthorship W3173194772A5044828935 @default.
- W3173194772 hasAuthorship W3173194772A5091538795 @default.
- W3173194772 hasBestOaLocation W31731947721 @default.
- W3173194772 hasConcept C104317684 @default.
- W3173194772 hasConcept C105702510 @default.
- W3173194772 hasConcept C129536746 @default.
- W3173194772 hasConcept C135073763 @default.
- W3173194772 hasConcept C145103041 @default.
- W3173194772 hasConcept C170774537 @default.
- W3173194772 hasConcept C193252679 @default.
- W3173194772 hasConcept C196843134 @default.
- W3173194772 hasConcept C197849852 @default.
- W3173194772 hasConcept C2777164004 @default.
- W3173194772 hasConcept C2777343278 @default.
- W3173194772 hasConcept C2777738586 @default.
- W3173194772 hasConcept C2780594696 @default.
- W3173194772 hasConcept C2780915607 @default.
- W3173194772 hasConcept C31507581 @default.
- W3173194772 hasConcept C54355233 @default.