Osteosarcoma inheritance in two families of Scottish deerhounds.

Canine genetics and epidemiology Pub Date : 2017-03-17 eCollection Date: 2017-01-01 DOI:10.1186/s40575-017-0042-8
John E Dillberger, Sara Ann McAtee
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引用次数: 7

Abstract

Background: Osteosarcoma is the most common neoplastic disease in Scottish Deerhounds. For Deerhounds, a 2007 population-based study concluded that a single dominant genetic factor largely governed disease risk. For Greyhounds, Rottweilers, and Irish Wolfhounds, a 2013 genome-wide association study found multiple genetic markers in each breed, with each marker only weakly associated with the disease. We obtained from two breeders the pedigrees, age (if alive) or age at death, and osteosarcoma status for two families of Scottish Deerhounds, designated Cohorts K and T. A dog was considered unaffected only if it was osteosarcoma-free and at least 8.5 years old. We analyzed the data in two ways, by assuming either a single recessive genetic factor or a single dominant genetic factor with high penetrance.

Results: Cohort K contained 54 evaluable dogs representing 12 litters. Cohort T contained 56 evaluable dogs representing eight litters. Osteosarcoma seemed clearly heritable in both cohorts; however, having a parent with osteosarcoma raised a pup's risk of developing osteosarcoma to 38% for Cohort K but 78% for Cohort T, suggesting the possibility of different genetic risk factors in each cohort. In Cohort K, osteosarcoma inheritance fit well with a single, recessive, autosomal risk factor, although we could not rule out the possibility of a single dominant risk factor with incomplete penetrance. In Cohort T, inheritance could be explained well by a single, dominant, autosomal risk factor but was inconsistent with recessive expression.

Conclusions: Inheritance of osteosarcoma in two Scottish Deerhound families could be explained well by a single genetic risk factor residing on an autosome, consistent with a 2007 report. In one family, inheritance was consistent with dominant expression, as previously reported. In the other family, inheritance fit better with recessive expression, although the possibility of a dominant genetic factor influenced by one or more other genetic factors could not be ruled out. In either case, the results suggest that there may be at least two different genetic risk factors for osteosarcoma in Deerhounds.

Abstract Image

Abstract Image

两个苏格兰猎鹿犬家族的骨肉瘤遗传。
背景:骨肉瘤是苏格兰猎鹿最常见的肿瘤疾病。对猎鹿犬来说,2007年的一项基于种群的研究得出结论,单一的显性遗传因素在很大程度上控制了疾病风险。对于灰狗、罗威纳犬和爱尔兰猎狼犬,2013年的一项全基因组关联研究发现,每个品种都有多个遗传标记,每个标记与疾病的关联都很弱。我们从两个饲养员那里获得了两个苏格兰猎鹿家族的血统、年龄(如果活着)或死亡年龄以及骨肉瘤状况,指定为队列K和t。只有当狗没有骨肉瘤且至少8.5岁时才被认为未受影响。我们以两种方式分析数据,通过假设一个单一的隐性遗传因素或一个单一的显性遗传因素具有高外显率。结果:队列K包含54只可评估的狗,代表12窝。队列T包含56只可评估的狗,代表8窝狗。在这两个队列中,骨肉瘤似乎明显具有遗传性;然而,如果父母一方患有骨肉瘤,幼崽患骨肉瘤的风险在队列K中为38%,在队列T中为78%,这表明每个队列中可能存在不同的遗传风险因素。在队列K中,骨肉瘤遗传与单个隐性常染色体风险因素吻合良好,尽管我们不能排除单个显性风险因素具有不完全外显率的可能性。在队列T中,遗传可以很好地解释为单一的显性常染色体危险因素,但与隐性表达不一致。结论:两个苏格兰猎鹿犬家族骨肉瘤的遗传可以通过驻留在常染色体上的单一遗传风险因素来很好地解释,与2007年的报告一致。如前所述,在一个家庭中,遗传与显性表达一致。在另一个家族中,遗传更符合隐性表达,尽管不能排除显性遗传因素受到一种或多种其他遗传因素影响的可能性。在任何一种情况下,结果表明,可能至少有两种不同的遗传风险因素导致猎犬骨肉瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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