The role of Bicoid cooperative binding in the patterning of sharp borders in Drosophila melanogaster

In Drosophila embryonic development, the Bicoid (Bcd) protein establishes positional information of downstream developmental genes like hunchback (hb), which has a strong anterior expression and a sharp on-off boundary in the mid-embryo. The role of Bcd cooperative binding in the positioning of the...

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Veröffentlicht in:Developmental biology 2012-10, Vol.370 (2), p.165-172
Hauptverfasser: Lopes, Francisco J.P, Spirov, Alexander V, Bisch, Paulo M
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Bisch, Paulo M
description In Drosophila embryonic development, the Bicoid (Bcd) protein establishes positional information of downstream developmental genes like hunchback (hb), which has a strong anterior expression and a sharp on-off boundary in the mid-embryo. The role of Bcd cooperative binding in the positioning of the Hb pattern has been previously demonstrated. However, there are discrepancies in the reported results about the role of this mechanism in the sharp Hb border. Here, we determined the Hill coefficient (nH) required for Bcd to generate the sharp border of Hb in wild-type (WT) embryos. We found that an nH of approximately 6.3 (s.d. 1.4) and 10.8 (s.d. 4.0) is required to account for Hb sharpness at early and late cycle 14A, respectively. Additional mechanisms are possibly required because the high nH is likely unachievable for Bcd binding to the hb promoter. To test this idea, we determined the nH required to pattern the Hb profile of 15 embryos expressing an hb14F allele that is defective in self-activation and found nH to be 3.0 (s.d. 1.0). This result indicates that in WT embryos, the hb self-activation is important for Hb sharpness. Corroborating our results, we also found a progressive increase in the required value of nH spanning from 4.0 to 9.2 by determining this coefficient from averaged profiles of eight temporal classes at cycle 14A (T1 to T8). Our results indicate that there is a transition in the mechanisms responsible for the sharp Hb border during cycle 14A: in early stages of this cycle, Bcd cooperative binding is primarily responsible for Hb sharpness; in late cycle 14A, hb self-activation becomes the dominant mechanism. [Display omitted] ► Bcd cooperative binding to the native hunchback promoter exhibits a Hill coefficient of approximately 3.0. ► A Hill coefficient of approximately 10.0 is necessary for sharp, mature Hunchback patterning. ► Bicoid cooperative binding cannot account for sharpness in the mature Hunchback pattern. ► Self-activation of hunchback is necessary to produce the sharp border of the mature Hunchback pattern.
doi_str_mv 10.1016/j.ydbio.2012.07.020
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The role of Bcd cooperative binding in the positioning of the Hb pattern has been previously demonstrated. However, there are discrepancies in the reported results about the role of this mechanism in the sharp Hb border. Here, we determined the Hill coefficient (nH) required for Bcd to generate the sharp border of Hb in wild-type (WT) embryos. We found that an nH of approximately 6.3 (s.d. 1.4) and 10.8 (s.d. 4.0) is required to account for Hb sharpness at early and late cycle 14A, respectively. Additional mechanisms are possibly required because the high nH is likely unachievable for Bcd binding to the hb promoter. To test this idea, we determined the nH required to pattern the Hb profile of 15 embryos expressing an hb14F allele that is defective in self-activation and found nH to be 3.0 (s.d. 1.0). This result indicates that in WT embryos, the hb self-activation is important for Hb sharpness. Corroborating our results, we also found a progressive increase in the required value of nH spanning from 4.0 to 9.2 by determining this coefficient from averaged profiles of eight temporal classes at cycle 14A (T1 to T8). Our results indicate that there is a transition in the mechanisms responsible for the sharp Hb border during cycle 14A: in early stages of this cycle, Bcd cooperative binding is primarily responsible for Hb sharpness; in late cycle 14A, hb self-activation becomes the dominant mechanism. 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Corroborating our results, we also found a progressive increase in the required value of nH spanning from 4.0 to 9.2 by determining this coefficient from averaged profiles of eight temporal classes at cycle 14A (T1 to T8). Our results indicate that there is a transition in the mechanisms responsible for the sharp Hb border during cycle 14A: in early stages of this cycle, Bcd cooperative binding is primarily responsible for Hb sharpness; in late cycle 14A, hb self-activation becomes the dominant mechanism. [Display omitted] ► Bcd cooperative binding to the native hunchback promoter exhibits a Hill coefficient of approximately 3.0. ► A Hill coefficient of approximately 10.0 is necessary for sharp, mature Hunchback patterning. ► Bicoid cooperative binding cannot account for sharpness in the mature Hunchback pattern. ► Self-activation of hunchback is necessary to produce the sharp border of the mature Hunchback pattern.</description><subject>alleles</subject><subject>Animals</subject><subject>Bicoid</subject><subject>Body Patterning</subject><subject>Cooperative binding</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - embryology</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila Proteins - metabolism</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>embryogenesis</subject><subject>Genes, Developmental</subject><subject>Hill coefficient</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Hunchback</subject><subject>Self-regulation</subject><subject>Trans-Activators - metabolism</subject><subject>Transcription Factors - metabolism</subject><issn>0012-1606</issn><issn>1095-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU-LFDEQxYMo7jj6CQTto5duq5L-e1DQdVeFBQ-O4C2kk8pMhp5Om_QM7Lc37ayLXsRcClK_eryqx9hzhAIB69f74tb0zhcckBfQFMDhAVshdFVe1eX3h2wFqZNjDfUFexLjHgBE24rH7ILztsS65CtmNjvKgh8o8zZ777R3JtPeTxTU7E6U9W40btxmbszmRE5qnimMy0_i406FKet9MBTignwIPvpp5waVHWhQo9-qmPin7JFVQ6Rnd3XNNtdXm8tP-c2Xj58v393kusJ6zlHwGitbAjVoDVXAOyMMtboW3CCvemvQWtuVChTqEi2iaqgreVkpjZVYs7dn2enYH8hoGuegBjkFd1DhVnrl5N-d0e3k1p-kKEuxvDV7dScQ_I8jxVkeXNQ0pE3IH6PEFgQ0dYP_gYLo2rZpqiah4ozqdJ0YyN47QpBLknIvfyUplyQlNDIlmaZe_LnM_czv6BLw8gxY5aXaBhflt69JoU4xt6KCxeObM0Hp5idHQUbtaNRkXCA9S-PdPy38BPW-uyQ</recordid><startdate>20121015</startdate><enddate>20121015</enddate><creator>Lopes, Francisco J.P</creator><creator>Spirov, Alexander V</creator><creator>Bisch, Paulo M</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20121015</creationdate><title>The role of Bicoid cooperative binding in the patterning of sharp borders in Drosophila melanogaster</title><author>Lopes, Francisco J.P ; 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The role of Bcd cooperative binding in the positioning of the Hb pattern has been previously demonstrated. However, there are discrepancies in the reported results about the role of this mechanism in the sharp Hb border. Here, we determined the Hill coefficient (nH) required for Bcd to generate the sharp border of Hb in wild-type (WT) embryos. We found that an nH of approximately 6.3 (s.d. 1.4) and 10.8 (s.d. 4.0) is required to account for Hb sharpness at early and late cycle 14A, respectively. Additional mechanisms are possibly required because the high nH is likely unachievable for Bcd binding to the hb promoter. To test this idea, we determined the nH required to pattern the Hb profile of 15 embryos expressing an hb14F allele that is defective in self-activation and found nH to be 3.0 (s.d. 1.0). This result indicates that in WT embryos, the hb self-activation is important for Hb sharpness. Corroborating our results, we also found a progressive increase in the required value of nH spanning from 4.0 to 9.2 by determining this coefficient from averaged profiles of eight temporal classes at cycle 14A (T1 to T8). Our results indicate that there is a transition in the mechanisms responsible for the sharp Hb border during cycle 14A: in early stages of this cycle, Bcd cooperative binding is primarily responsible for Hb sharpness; in late cycle 14A, hb self-activation becomes the dominant mechanism. [Display omitted] ► Bcd cooperative binding to the native hunchback promoter exhibits a Hill coefficient of approximately 3.0. ► A Hill coefficient of approximately 10.0 is necessary for sharp, mature Hunchback patterning. ► Bicoid cooperative binding cannot account for sharpness in the mature Hunchback pattern. ► Self-activation of hunchback is necessary to produce the sharp border of the mature Hunchback pattern.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22841642</pmid><doi>10.1016/j.ydbio.2012.07.020</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects alleles
Animals
Bicoid
Body Patterning
Cooperative binding
DNA-Binding Proteins - metabolism
Drosophila melanogaster
Drosophila melanogaster - embryology
Drosophila melanogaster - metabolism
Drosophila Proteins - metabolism
Embryo, Nonmammalian - metabolism
embryogenesis
Genes, Developmental
Hill coefficient
Homeodomain Proteins - metabolism
Hunchback
Self-regulation
Trans-Activators - metabolism
Transcription Factors - metabolism
title The role of Bicoid cooperative binding in the patterning of sharp borders in Drosophila melanogaster
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