{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T02:04:22Z","timestamp":1789524262064,"version":"build-2803163510"},"reference-count":16,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2011,5,27]],"date-time":"2011-05-27T00:00:00Z","timestamp":1306454400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Animal Genetics"],"published-print":{"date-parts":[[2012,2]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Mutations in the gene encoding fibrillin\u20101 (<jats:italic>FBN1<\/jats:italic>), a component of the extracellular microfibril, cause Marfan syndrome (MFS). Frequent observation of cattle with a normal withers height, but lower body weight than age\u2010matched normal cattle, was recently reported among cattle sired by phenotypically normal Bull A, in Japanese Black cattle. These cattle also showed other characteristic features similar to the clinical phenotype of human MFS, such as a long phalanx proximalis, oval face and crystalline lens cloudiness. We first screened a paternal half\u2010sib family comprising 36 affected and 10 normal offspring of Bull A using the BovineSNP50 BeadChip (illumina). Twenty\u2010two microsatellite markers mapped to a significant region on BTA10 were subsequently genotyped on the family. The bovine Marfan syndrome\u2010like disease (MFSL) was mapped onto BTA10. As <jats:italic>FBN1<\/jats:italic> is located in the significant region, <jats:italic>FBN1<\/jats:italic> was sequenced in Bull A, and three affected and one normal cattle. A G&gt;A mutation at the intron64 splicing accepter site (c.8227\u20101G&gt;A) was detected in 31 of 36 affected animals (84.7%). The c.8227\u20101G&gt;A polymorphism was not found in 20 normal offspring of Bull A or in 93 normal cattle unrelated to Bull A. The mutation caused a 1\u2010base shift of the intron64 splicing accepter site to the 3\u2032 direction, and a 1\u2010base deletion in processed mRNA. This 1\u2010base deletion creates a premature termination codon, and a 125\u2010amino acid shorter Fibrillin\u20101 protein is produced from the mutant mRNA. We therefore conclude that the c.8227\u20101G&gt;A mutation is causative for MFSL. Furthermore, it was suggested that Bull A exhibited germline mosaicism for the mutation, and that the frequency of the mutant sperm was 14.9%.<\/jats:p>","DOI":"10.1111\/j.1365-2052.2011.02209.x","type":"journal-article","created":{"date-parts":[[2011,5,27]],"date-time":"2011-05-27T13:49:01Z","timestamp":1306504141000},"page":"11-17","source":"Crossref","is-referenced-by-count":31,"title":["Identification of an <i>FBN1<\/i> mutation in bovine Marfan syndrome\u2010like disease"],"prefix":"10.1111","volume":"43","author":[{"given":"T.","family":"Hirano","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T.","family":"Matsuhashi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N.","family":"Kobayashi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T.","family":"Watanabe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y.","family":"Sugimoto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2011,5,27]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1253\/circj.71.1305"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1093\/genetics\/138.3.963"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/352337a0"},{"key":"e_1_2_5_5_1","doi-asserted-by":"crossref","first-page":"1195","DOI":"10.1093\/genetics\/136.3.1195","article-title":"Mapping QTL in crosses between outbred lines using least squares","volume":"136","author":"Haley C.S.","year":"1994","journal-title":"Genetics"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2052.1996.tb00980.x"},{"key":"e_1_2_5_7_1","doi-asserted-by":"publisher","DOI":"10.1101\/gr.2741704"},{"key":"e_1_2_5_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(05)67789-6"},{"key":"e_1_2_5_9_1","doi-asserted-by":"publisher","DOI":"10.1101\/gr.7.3.235"},{"key":"e_1_2_5_10_1","doi-asserted-by":"publisher","DOI":"10.1098\/rstb.2001.1029"},{"key":"e_1_2_5_11_1","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.M409029200"},{"key":"e_1_2_5_12_1","first-page":"8","article-title":"Fifteen novel FBN1 mutation causing Marfan syndrome detected by heteroduplex analysis of genomic amplifications","volume":"57","author":"Nijbroek G.","year":"1995","journal-title":"American Journal of Human Genetics"},{"key":"e_1_2_5_13_1","doi-asserted-by":"publisher","DOI":"10.1002\/humu.10113"},{"key":"e_1_2_5_14_1","doi-asserted-by":"publisher","DOI":"10.1093\/bioinformatics\/18.2.339"},{"key":"e_1_2_5_15_1","doi-asserted-by":"publisher","DOI":"10.1002\/humu.20152"},{"key":"e_1_2_5_16_1","doi-asserted-by":"publisher","DOI":"10.1093\/genetics\/143.2.1013"},{"key":"e_1_2_5_17_1","doi-asserted-by":"crossref","first-page":"1417","DOI":"10.1093\/genetics\/143.3.1417","article-title":"Mapping quantitative trait loci for complex binary diseases using line crosses","volume":"143","author":"Xu S.","year":"1996","journal-title":"Genetics"}],"container-title":["Animal Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1365-2052.2011.02209.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/j.1365-2052.2011.02209.x","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,31]],"date-time":"2023-10-31T00:45:45Z","timestamp":1698713145000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1365-2052.2011.02209.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,5,27]]},"references-count":16,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2012,2]]}},"alternative-id":["10.1111\/j.1365-2052.2011.02209.x"],"URL":"https:\/\/doi.org\/10.1111\/j.1365-2052.2011.02209.x","archive":["Portico"],"relation":{},"ISSN":["0268-9146","1365-2052"],"issn-type":[{"value":"0268-9146","type":"print"},{"value":"1365-2052","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,5,27]]}}}