Loading…
The serine/threonine kinase, Krct, affects endbud morphogenesis during murine mammary gland development
STK16/Krct (Kinase related to cerevisiae and thaliana) is a ubiquitously expressed member of a unique family of serine/threonine protein kinases that is conserved among all eukaryotes. Despite its cloning 6 years ago to date, the function of this kinase remains unknown. In an attempt to identify a f...
Saved in:
Published in: | Transgenic research 2005-12, Vol.14 (6), p.919-940 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c357t-b923abc356380d0f688b516e5ae9e236bea8fd4bdc40b0bd69d8f2fd7d5d6f2a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c357t-b923abc356380d0f688b516e5ae9e236bea8fd4bdc40b0bd69d8f2fd7d5d6f2a3 |
container_end_page | 940 |
container_issue | 6 |
container_start_page | 919 |
container_title | Transgenic research |
container_volume | 14 |
creator | Stairs, Douglas B Notarfrancesco, Kathleen L Chodosh, Lewis A |
description | STK16/Krct (Kinase related to cerevisiae and thaliana) is a ubiquitously expressed member of a unique family of serine/threonine protein kinases that is conserved among all eukaryotes. Despite its cloning 6 years ago to date, the function of this kinase remains unknown. In an attempt to identify a function for Krct, we have generated a doxycycline-dependent transgenic mouse model that permits the inducible overexpression of Krct in the mammary glands of mice treated with tetracycline derivatives. Analysis of these mice reveals that modest overexpression of Krct in the mammary gland during puberty results in duplication of the terminal endbud axis such that multiple, rather than single, budding structures arise at the ends of primary ducts. Supernumerary endbuds in Krct overexpressing mice resemble wild-type terminal endbuds with regard to cellular proliferation rates and localization of cap cells, myoepithelial cells and body cells. However, aberrant transgenic endbuds are surrounded by an increased amount of periductal stroma that in many cases encompasses the entire endbud. These data suggest that Krct may play a role in regulating stromal-epithelial interactions that occur during ductal morphogenesis in the mammary gland. |
doi_str_mv | 10.1007/s11248-005-1806-6 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68844851</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19734818</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-b923abc356380d0f688b516e5ae9e236bea8fd4bdc40b0bd69d8f2fd7d5d6f2a3</originalsourceid><addsrcrecordid>eNqFkU9LwzAYh4MoOqcfwIsED55WlzRNmh5l-A8HXuY5JM2brnNtZ9IKfntTNhC8eHpfyPP7keRB6IqSO0pIPg-UpplMCOEJlUQk4ghNKM9ZUjAhj9GEFCJNpKTFGToPYUNITEl2is6oYJTH0wmqVmvAAXzdwrxfe-jauOGPutUBZvjVl_0Ma-eg7AOG1prB4qbzu3VXQQuhDtgOMVvhZhyAG9002n_jaqtbiy18wbbbNdD2F-jE6W2Ay8OcovfHh9XiOVm-Pb0s7pdJyXjeJ6ZImTZxF0wSS5yQ0nAqgGsoIGXCgJbOZsaWGTHEWFFY6VJnc8utcKlmU3S779357nOA0KumDiVs432gG4KKhVkmOf0XpEXOMkllBG_-gJtu8G18hMp5SiTlRRYhuodK34Xgwamdr8efUJSo0ZXau1LRlRpdKREz14fiwTRgfxMHOewHodyQ4w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>752081594</pqid></control><display><type>article</type><title>The serine/threonine kinase, Krct, affects endbud morphogenesis during murine mammary gland development</title><source>Springer Nature</source><creator>Stairs, Douglas B ; Notarfrancesco, Kathleen L ; Chodosh, Lewis A</creator><creatorcontrib>Stairs, Douglas B ; Notarfrancesco, Kathleen L ; Chodosh, Lewis A</creatorcontrib><description>STK16/Krct (Kinase related to cerevisiae and thaliana) is a ubiquitously expressed member of a unique family of serine/threonine protein kinases that is conserved among all eukaryotes. Despite its cloning 6 years ago to date, the function of this kinase remains unknown. In an attempt to identify a function for Krct, we have generated a doxycycline-dependent transgenic mouse model that permits the inducible overexpression of Krct in the mammary glands of mice treated with tetracycline derivatives. Analysis of these mice reveals that modest overexpression of Krct in the mammary gland during puberty results in duplication of the terminal endbud axis such that multiple, rather than single, budding structures arise at the ends of primary ducts. Supernumerary endbuds in Krct overexpressing mice resemble wild-type terminal endbuds with regard to cellular proliferation rates and localization of cap cells, myoepithelial cells and body cells. However, aberrant transgenic endbuds are surrounded by an increased amount of periductal stroma that in many cases encompasses the entire endbud. These data suggest that Krct may play a role in regulating stromal-epithelial interactions that occur during ductal morphogenesis in the mammary gland.</description><identifier>ISSN: 0962-8819</identifier><identifier>EISSN: 1573-9368</identifier><identifier>DOI: 10.1007/s11248-005-1806-6</identifier><identifier>PMID: 16315096</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Animals ; Apoptosis ; Cell Proliferation ; DNA-Binding Proteins - physiology ; Epithelial Cells - cytology ; Epithelial Cells - physiology ; Female ; Male ; Mammary Glands, Animal - growth & development ; Mammary Glands, Animal - metabolism ; Mice ; Mice, Transgenic ; Morphogenesis ; Protein-Serine-Threonine Kinases - physiology ; Proteins ; Rodents ; Stromal Cells - cytology ; Stromal Cells - physiology ; Transcription Factors - physiology</subject><ispartof>Transgenic research, 2005-12, Vol.14 (6), p.919-940</ispartof><rights>Springer 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-b923abc356380d0f688b516e5ae9e236bea8fd4bdc40b0bd69d8f2fd7d5d6f2a3</citedby><cites>FETCH-LOGICAL-c357t-b923abc356380d0f688b516e5ae9e236bea8fd4bdc40b0bd69d8f2fd7d5d6f2a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16315096$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stairs, Douglas B</creatorcontrib><creatorcontrib>Notarfrancesco, Kathleen L</creatorcontrib><creatorcontrib>Chodosh, Lewis A</creatorcontrib><title>The serine/threonine kinase, Krct, affects endbud morphogenesis during murine mammary gland development</title><title>Transgenic research</title><addtitle>Transgenic Res</addtitle><description>STK16/Krct (Kinase related to cerevisiae and thaliana) is a ubiquitously expressed member of a unique family of serine/threonine protein kinases that is conserved among all eukaryotes. Despite its cloning 6 years ago to date, the function of this kinase remains unknown. In an attempt to identify a function for Krct, we have generated a doxycycline-dependent transgenic mouse model that permits the inducible overexpression of Krct in the mammary glands of mice treated with tetracycline derivatives. Analysis of these mice reveals that modest overexpression of Krct in the mammary gland during puberty results in duplication of the terminal endbud axis such that multiple, rather than single, budding structures arise at the ends of primary ducts. Supernumerary endbuds in Krct overexpressing mice resemble wild-type terminal endbuds with regard to cellular proliferation rates and localization of cap cells, myoepithelial cells and body cells. However, aberrant transgenic endbuds are surrounded by an increased amount of periductal stroma that in many cases encompasses the entire endbud. These data suggest that Krct may play a role in regulating stromal-epithelial interactions that occur during ductal morphogenesis in the mammary gland.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Cell Proliferation</subject><subject>DNA-Binding Proteins - physiology</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - physiology</subject><subject>Female</subject><subject>Male</subject><subject>Mammary Glands, Animal - growth & development</subject><subject>Mammary Glands, Animal - metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Morphogenesis</subject><subject>Protein-Serine-Threonine Kinases - physiology</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Stromal Cells - cytology</subject><subject>Stromal Cells - physiology</subject><subject>Transcription Factors - physiology</subject><issn>0962-8819</issn><issn>1573-9368</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkU9LwzAYh4MoOqcfwIsED55WlzRNmh5l-A8HXuY5JM2brnNtZ9IKfntTNhC8eHpfyPP7keRB6IqSO0pIPg-UpplMCOEJlUQk4ghNKM9ZUjAhj9GEFCJNpKTFGToPYUNITEl2is6oYJTH0wmqVmvAAXzdwrxfe-jauOGPutUBZvjVl_0Ma-eg7AOG1prB4qbzu3VXQQuhDtgOMVvhZhyAG9002n_jaqtbiy18wbbbNdD2F-jE6W2Ay8OcovfHh9XiOVm-Pb0s7pdJyXjeJ6ZImTZxF0wSS5yQ0nAqgGsoIGXCgJbOZsaWGTHEWFFY6VJnc8utcKlmU3S779357nOA0KumDiVs432gG4KKhVkmOf0XpEXOMkllBG_-gJtu8G18hMp5SiTlRRYhuodK34Xgwamdr8efUJSo0ZXau1LRlRpdKREz14fiwTRgfxMHOewHodyQ4w</recordid><startdate>200512</startdate><enddate>200512</enddate><creator>Stairs, Douglas B</creator><creator>Notarfrancesco, Kathleen L</creator><creator>Chodosh, Lewis A</creator><general>Springer Nature B.V</general><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>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>200512</creationdate><title>The serine/threonine kinase, Krct, affects endbud morphogenesis during murine mammary gland development</title><author>Stairs, Douglas B ; Notarfrancesco, Kathleen L ; Chodosh, Lewis A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-b923abc356380d0f688b516e5ae9e236bea8fd4bdc40b0bd69d8f2fd7d5d6f2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Cell Proliferation</topic><topic>DNA-Binding Proteins - physiology</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - physiology</topic><topic>Female</topic><topic>Male</topic><topic>Mammary Glands, Animal - growth & development</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Morphogenesis</topic><topic>Protein-Serine-Threonine Kinases - physiology</topic><topic>Proteins</topic><topic>Rodents</topic><topic>Stromal Cells - cytology</topic><topic>Stromal Cells - physiology</topic><topic>Transcription Factors - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stairs, Douglas B</creatorcontrib><creatorcontrib>Notarfrancesco, Kathleen L</creatorcontrib><creatorcontrib>Chodosh, Lewis A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transgenic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stairs, Douglas B</au><au>Notarfrancesco, Kathleen L</au><au>Chodosh, Lewis A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The serine/threonine kinase, Krct, affects endbud morphogenesis during murine mammary gland development</atitle><jtitle>Transgenic research</jtitle><addtitle>Transgenic Res</addtitle><date>2005-12</date><risdate>2005</risdate><volume>14</volume><issue>6</issue><spage>919</spage><epage>940</epage><pages>919-940</pages><issn>0962-8819</issn><eissn>1573-9368</eissn><abstract>STK16/Krct (Kinase related to cerevisiae and thaliana) is a ubiquitously expressed member of a unique family of serine/threonine protein kinases that is conserved among all eukaryotes. Despite its cloning 6 years ago to date, the function of this kinase remains unknown. In an attempt to identify a function for Krct, we have generated a doxycycline-dependent transgenic mouse model that permits the inducible overexpression of Krct in the mammary glands of mice treated with tetracycline derivatives. Analysis of these mice reveals that modest overexpression of Krct in the mammary gland during puberty results in duplication of the terminal endbud axis such that multiple, rather than single, budding structures arise at the ends of primary ducts. Supernumerary endbuds in Krct overexpressing mice resemble wild-type terminal endbuds with regard to cellular proliferation rates and localization of cap cells, myoepithelial cells and body cells. However, aberrant transgenic endbuds are surrounded by an increased amount of periductal stroma that in many cases encompasses the entire endbud. These data suggest that Krct may play a role in regulating stromal-epithelial interactions that occur during ductal morphogenesis in the mammary gland.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>16315096</pmid><doi>10.1007/s11248-005-1806-6</doi><tpages>22</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0962-8819 |
ispartof | Transgenic research, 2005-12, Vol.14 (6), p.919-940 |
issn | 0962-8819 1573-9368 |
language | eng |
recordid | cdi_proquest_miscellaneous_68844851 |
source | Springer Nature |
subjects | Animals Apoptosis Cell Proliferation DNA-Binding Proteins - physiology Epithelial Cells - cytology Epithelial Cells - physiology Female Male Mammary Glands, Animal - growth & development Mammary Glands, Animal - metabolism Mice Mice, Transgenic Morphogenesis Protein-Serine-Threonine Kinases - physiology Proteins Rodents Stromal Cells - cytology Stromal Cells - physiology Transcription Factors - physiology |
title | The serine/threonine kinase, Krct, affects endbud morphogenesis during murine mammary gland development |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T17%3A26%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20serine/threonine%20kinase,%20Krct,%20affects%20endbud%20morphogenesis%20during%20murine%20mammary%20gland%20development&rft.jtitle=Transgenic%20research&rft.au=Stairs,%20Douglas%20B&rft.date=2005-12&rft.volume=14&rft.issue=6&rft.spage=919&rft.epage=940&rft.pages=919-940&rft.issn=0962-8819&rft.eissn=1573-9368&rft_id=info:doi/10.1007/s11248-005-1806-6&rft_dat=%3Cproquest_cross%3E19734818%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c357t-b923abc356380d0f688b516e5ae9e236bea8fd4bdc40b0bd69d8f2fd7d5d6f2a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=752081594&rft_id=info:pmid/16315096&rfr_iscdi=true |