Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation.

ABSTRACT:

Rationale

Primary ciliary dyskinesia (PCD) is a rare, usually autosomal recessive, genetic disorder characterized by ciliary dysfunction, sino-pulmonary disease, and situs inversus. Disease-causing mutations have been reported in DNAI1 and DNAH5 encoding outer dynein arm (ODA) proteins of cilia.

Objectives

We analyzed DNAI1 to identify disease-causing mutations in PCD and to determine if the previously reported IVS1+2_3insT (219+3insT) mutation represents a "founder" or "hot spot" mutation.

Methods

Patients with PCD from 179 unrelated families were studied. Exclusion mapping showed no linkage to DNAI1 for 13 families; the entire coding region was sequenced in a patient from the remaining 166 families. Reverse transcriptase-polymerase chain reaction (RT-PCR) was perfor

SUBMITTER: Zariwala MA 

PROVIDER: S-EPMC2648054 | biostudies-literature | 2006 Oct

REPOSITORIES: biostudies-literature